{
"NDC": [
{
"NDCCode": "43742-1325-4",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-1325-4) ",
"NDC11Code": "43742-1325-04",
"ProductNDC": "43742-1325",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Rheumagesic",
"NonProprietaryName": "Arnica Montana, Apis Mellifica, Benzoicum Acidum, Cartilago Suis, Ledum Palustre, Pantothenic Acid, Ruta Graveolens, Rhododendron Chrysanthum, Causticum, Formica Rufa, Sepia, Alpha-lipoicum Acidum, Aurum Metallicum, Calcarea Phosphorica, Colchicum Autumnale, Phytolacca Decandra, Radium Bromatum, Rhus Venenata, Thuja Occidentalis, Lac Caninum",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20190109",
"EndMarketingDate": "20251008",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "APIS MELLIFERA; ARNICA MONTANA; BENZOIC ACID; CANIS LUPUS FAMILIARIS MILK; CAUSTICUM; COLCHICUM AUTUMNALE BULB; FORMICA RUFA; GOLD; PANTOTHENIC ACID; PHYTOLACCA AMERICANA ROOT; RADIUM BROMIDE; RHODODENDRON AUREUM LEAF; RHODODENDRON TOMENTOSUM LEAFY TWIG; RUTA GRAVEOLENS FLOWERING TOP; SEPIA OFFICINALIS JUICE; SUS SCROFA CARTILAGE; THIOCTIC ACID; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON VERNIX LEAFY TWIG; TRIBASIC CALCIUM PHOSPHATE",
"StrengthNumber": "6; 3; 6; 16; 10; 12; 10; 12; 6; 12; 12; 8; 6; 6; 10; 6; 12; 12; 12; 12",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Pharm_Classes": "Allergens [CS], Allergens [CS], Ammonium Ion Binding Activity [MoA], Bee Venoms [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nitrogen Binding Agent [EPC], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC]",
"Status": "Deprecated",
"LastUpdate": "2025-10-08",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20190109",
"EndMarketingDatePackage": "20251008",
"SamplePackage": "N",
"IndicationAndUsage": "For temporary relief of symptoms related to arthritis including swelling, joint pain, back pain, inflammation in joints and muscle pain. **. **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration."
},
{
"NDCCode": "43742-0702-4",
"PackageDescription": "960 mL in 1 BOTTLE (43742-0702-4)",
"NDC11Code": "43742-0702-04",
"ProductNDC": "43742-0702",
"ProductTypeName": "DRUG FOR FURTHER PROCESSING",
"NonProprietaryName": "Aconitum Napellus, Antimonium Tartaricum, Arsenicum Iodatum, Belladonna, Bryonia, Causticum, Coccus Cacti, Cuprum Aceticum, Drosera (rotundifolia), Hyoscyamus Niger, Ipecacuanha, Kreosotum, Lobelia Inflata, Phosphorus, Scilla Maritima, Sticta Pulmonaria, Silicea, Carbo Vegetabilis, Kali Carbonicum, Lachesis Mutus, Pertussinum, Tetanus Toxin",
"DosageFormName": "LIQUID",
"StartMarketingDate": "20151230",
"EndMarketingDate": "20220123",
"MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
"LabelerName": "Deseret Biologicals",
"SubstanceName": "ACONITUM NAPELLUS; ANTIMONY POTASSIUM TARTRATE; ARSENIC TRIIODIDE; ATROPA BELLADONNA; BRYONIA ALBA ROOT; CAUSTICUM; PROTORTONIA CACTI; CUPRIC ACETATE; DROSERA ROTUNDIFOLIA; HYOSCYAMUS NIGER; IPECAC; WOOD CREOSOTE; LOBELIA INFLATA; PHOSPHORUS; DRIMIA MARITIMA BULB; LOBARIA PULMONARIA; SILICON DIOXIDE; ACTIVATED CHARCOAL; POTASSIUM CARBONATE; LACHESIS MUTA VENOM; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; TETANUS TOXIN",
"StrengthNumber": "6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 12; 12; 12; 30; 32",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2014-02-04",
"ListingRecordCertifiedThrough": "20181231"
},
{
"NDCCode": "22840-1325-4",
"PackageDescription": "50 mL in 1 VIAL, MULTI-DOSE (22840-1325-4) ",
"NDC11Code": "22840-1325-04",
"ProductNDC": "22840-1325",
"ProductTypeName": "NON-STANDARDIZED ALLERGENIC",
"ProprietaryName": "Firebush Kochia",
"NonProprietaryName": "Kochia Scoparia",
"DosageFormName": "SOLUTION",
"RouteName": "INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS",
"StartMarketingDate": "19810915",
"MarketingCategoryName": "BLA",
"ApplicationNumber": "BLA101833",
"LabelerName": "Greer Laboratories, Inc.",
"SubstanceName": "BASSIA SCOPARIA POLLEN",
"StrengthNumber": ".1",
"StrengthUnit": "g/mL",
"Pharm_Classes": "Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS]",
"Status": "Active",
"LastUpdate": "2025-06-07",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "19810915",
"SamplePackage": "N",
"IndicationAndUsage": "Non-Standardized Allergenic Extracts are indicated for. : 1 Skin test diagnosis of patients with a clinical history of allergies to one or more of the specific non-standardized allergens., 2 Immunotherapy for the reduction of allergen-induced allergic symptoms confirmed by appropriate positive skin tests or by in vitro testing for allergen-specific IgE antibodies. .",
"Description": "Non-Standardized Allergenic Extracts are sterile solutions used for percutaneous testing, intradermal testing, or subcutaneous immunotherapy. Aqueous extracts contain the soluble extractants of the source material in water for injection, 0.5% sodium chloride, 0.54% sodium bicarbonate, and 0.4% phenol. Glycerinated extracts contain the soluable extractants of the source material in water for injection and 50% glycerin, 0.25% sodium chloride, 0.27% sodium bicarbonate, and 0.2% phenol. The pH of the extracts range from 6 to 9. Certain food extracts (Barley, Oat, Pineapple, Rye, Spinach, and Wheat), labeled “For Diagnostic Use Only”, contain 0.1% sodium formaldehyde sulfoxylate as an antioxidant. Source materials used in the manufacture of allergenic extracts are collected from natural sources or from laboratory cultures. Non-Standardized Allergenic Extracts appear as clear and colorless to dark brown solutions that should be free of particulate matter. Extracts are labeled either as weight-to-volume based on the weight of the source material to the volume of the extracting fluid, or as PNU/milliliter with one PNU representing 0.00001 mg of protein nitrogen per milliliter."
},
{
"NDCCode": "36987-1325-4",
"PackageDescription": "50 mL in 1 VIAL, MULTI-DOSE (36987-1325-4)",
"NDC11Code": "36987-1325-04",
"ProductNDC": "36987-1325",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Fig",
"NonProprietaryName": "Fig",
"DosageFormName": "INJECTION, SOLUTION",
"RouteName": "INTRADERMAL; SUBCUTANEOUS",
"StartMarketingDate": "19720829",
"MarketingCategoryName": "BLA",
"ApplicationNumber": "BLA102192",
"LabelerName": "Nelco Laboratories, Inc.",
"SubstanceName": "FIG",
"StrengthNumber": ".1",
"StrengthUnit": "g/mL",
"Pharm_Classes": "Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Fruit Proteins [EXT]",
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20171231",
"IndicationAndUsage": "Allergenic extracts are indicated for use in diagnostic testing and as part of a treatment regime for allergic disease, as established by allergy history and skin test reactivity. Allergenic extracts are indicated for the treatment of allergen specific allergic disease for use as hyposensitization or immunotherapy when avoidance of specific allergens can not be attained. The use of allergenic extracts for therapeutic purpose has been established by well-controlled clinical studies. Allergenic extracts may be used as adjunctive therapy along with pharmacotherapy which includes antihistamines, corticosteroids, and cromoglycate, and avoidance measures. Allergenic extracts for therapeutic use should be given using only the allergen selection to which the patient is allergic, has a history of exposure and are likely to be exposed to again.",
"Description": "Allergenic extracts are sterile solutions consisting of the extractable components from various biological sources including pollens, inhalants, molds, animal epidermals and insects. Aqueous extracts are prepared using cocas fluid containing NaCl 0.5%, NaHCO3 0.0275%, WFI, preservative 0.4% Phenol. Glycerinated allergenic extracts are prepared with cocas fluid and glycerin to produce a 50% (v/v) allergenic extract. Allergenic Extracts are supplied as concentrations designated as protein nitrogen units (PNU) or weight/volume (w/v) ratio. Standardized extracts are designated in Bioequivalent Allergy Units (BAU) or Allergy Units (AU). (See product insert for standardized extracts). For diagnostic purposes, allergenic extracts are to be administered by prick-puncture or intradermal routes. Allergenic extracts are administered subcutaneously for immunotherapy injections."
},
{
"NDCCode": "70771-1325-4",
"PackageDescription": "10 BLISTER PACK in 1 CARTON (70771-1325-4) / 10 TABLET in 1 BLISTER PACK (70771-1325-2) ",
"NDC11Code": "70771-1325-04",
"ProductNDC": "70771-1325",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Candesartan Cilexetil And Hydrochlorothiazide",
"NonProprietaryName": "Candesartan Cilexetil And Hydrochlorothiazide",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20180414",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA203466",
"LabelerName": "Zydus Lifesciences Limited",
"SubstanceName": "CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE",
"StrengthNumber": "16; 12.5",
"StrengthUnit": "mg/1; mg/1",
"Pharm_Classes": "Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]",
"Status": "Active",
"LastUpdate": "2024-11-14",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20180414",
"SamplePackage": "N"
},
{
"NDCCode": "71335-1325-4",
"PackageDescription": "10 CAPSULE in 1 BOTTLE (71335-1325-4) ",
"NDC11Code": "71335-1325-04",
"ProductNDC": "71335-1325",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Hydroxyzine Pamoate",
"NonProprietaryName": "Hydroxyzine Pamoate",
"DosageFormName": "CAPSULE",
"RouteName": "ORAL",
"StartMarketingDate": "20130603",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA201507",
"LabelerName": "Bryant Ranch Prepack",
"SubstanceName": "HYDROXYZINE PAMOATE",
"StrengthNumber": "25",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Antihistamine [EPC], Histamine Receptor Antagonists [MoA]",
"Status": "Active",
"LastUpdate": "2025-10-13",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20220919",
"SamplePackage": "N",
"IndicationAndUsage": "For symptomatic relief of anxiety and tension associated with psychoneurosis and as an adjunct in organic disease states in which anxiety is manifested. Useful in the management of pruritus due to allergic conditions such as chronic urticaria and atopic and contact dermatoses, and in histamine-mediated pruritus. As a sedative when used as premedication and following general anesthesia, Hydroxyzine may potentiate meperidine (Demerol®) and barbiturates, so their use in pre-anesthetic adjunctive therapy should be modified on an individual basis. Atropine and other belladonna alkaloids are not affected by the drug. Hydroxyzine is not known to interfere with the action of digitalis in any way and it may be used concurrently with this agent. The effectiveness of hydroxyzine as an antianxiety agent for long-term use, that is, more than 4 months, has not been assessed by systematic clinical studies. The physician should reassess periodically the usefulness of the drug for the individual patient.",
"Description": "Hydroxyzine pamoate is a light yellow odorless powder, practically insoluble in water and methanol and freely soluble in dimethylformamide. It is chemically designated as (±)-2-[2-[4-(p-Chloro-α-phenylbenzyl)-1-piperazinyl]ethoxy]ethanol 4,4 -methylenebis[3-hydroxy-2-naphthoate] (1:1) and can be structurally represented as follows. Chemical Formula: C21H27ClN2O2.C23H16O6. Molecular Weight: 763.29. Inert ingredients for the capsule formulations are: hard gelatin capsules (which contain gelatin, titanium dioxide, FD&C Blue #1, FD&C Red #40, D&C Yellow #10), printing ink which contains shellac glaze ~45% (20% esterified) in Ethanol, iron oxide black, n-butyl alcohol, isopropyl alcohol, propylene glycol and ammonium hydroxide 28%); magnesium stearate, microcrystalline cellulose, pregelatinized starch, sodium lauryl sulfate, sodium starch glycolate."
},
{
"NDCCode": "0115-1325-10",
"PackageDescription": "90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1325-10) ",
"NDC11Code": "00115-1325-10",
"ProductNDC": "0115-1325",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Fenofibric Acid",
"NonProprietaryName": "Fenofibric Acid",
"DosageFormName": "CAPSULE, DELAYED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20240601",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA200264",
"LabelerName": "Amneal Pharmaceuticals of New York LLC",
"SubstanceName": "FENOFIBRIC ACID",
"StrengthNumber": "135",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Peroxisome Proliferator Receptor alpha Agonist [EPC]",
"Status": "Active",
"LastUpdate": "2025-08-11",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20240601",
"SamplePackage": "N",
"IndicationAndUsage": "Fenofibric acid delayed-release capsules are indicated as adjunctive therapy to diet: 1 to reduce triglyceride (TG) levels in adults with severe hypertriglyceridemia (TG greater than or equal to 500 mg/dL)., 2 to reduce elevated low-density lipoprotein cholesterol (LDL-C) in adults with primary hyperlipidemia when use of recommended LDL-C lowering therapy is not possible.",
"Description": "Fenofibric acid is a peroxisome proliferator-activated receptor (PPAR) alpha agonist available as delayed-release capsules for oral administration. Each delayed-release capsule contains choline fenofibrate, equivalent to 45 mg or 135 mg of fenofibric acid. The chemical name for choline fenofibrate is ethanaminium, 2-hydroxy-N,N,N-trimethyl, 2-[4-(4-chlorobenzoyl)phenoxy]-2-methylpropanoate (1:1) with the following structural formula. The molecular formula is C22H28ClNO5 and the molecular weight is 421.91 g/mole. Choline fenofibrate is freely soluble in water and methanol. The melting point is approximately 210°C. Choline fenofibrate is a white to off-white powder, which is stable under ordinary conditions. Each delayed-release capsule contains enteric coated seeds comprised of choline fenofibrate and the following inactive ingredients: acetyltributyl citrate, ethylcellulose, hypromellose, hypromellose phthalate, microcrystalline cellulose, silicon dioxide, and talc. The capsule shell of the 45 mg capsule contains the following inactive ingredients: FD&C Red #40, FD&C yellow #5, FD&C Yellow #6, gelatin, and titanium dioxide. The capsule shell of the 135 mg capsule contains the following inactive ingredients: FD&C Blue #1, FD&C Red #3, FD&C Yellow #5, FD&C Yellow #6, gelatin and titanium dioxide. The capsule is imprinted with black pharmaceutical ink which includes butyl alcohol, dehydrated alcohol, ferrosoferric oxide, isopropyl alcohol, potassium hydroxide, propylene glycol, purified water, shellac, and strong ammonia solution."
},
{
"NDCCode": "51662-1325-1",
"PackageDescription": "1 mL in 1 VIAL, SINGLE-DOSE (51662-1325-1) ",
"NDC11Code": "51662-1325-01",
"ProductNDC": "51662-1325",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ephedrine Sulfate",
"NonProprietaryName": "Ephedrine Sulfate",
"DosageFormName": "INJECTION, SOLUTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20181021",
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA208943",
"LabelerName": "HF Acquisition Co LLC, DBA HealthFirst",
"SubstanceName": "EPHEDRINE SULFATE",
"StrengthNumber": "50",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Increased Norepinephrine Activity [PE], Norepinephrine Releasing Agent [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]",
"Status": "Active",
"LastUpdate": "2024-02-28",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20181021",
"SamplePackage": "N",
"IndicationAndUsage": "Ephedrine sulfate injection is indicated for the treatment of clinically important hypotension occurring in the setting of anesthesia.",
"Description": "Ephedrine sulfate is an alpha- and beta-adrenergic agonist and a norepinephrine-releasing agent. Ephedrine sulfate injection, USP is a clear, colorless, sterile solution for intravenous injection. Each mL contains ephedrine sulfate 50 mg in water for injection as a single-dose product. The pH range is 4.5 to 7.0. The drug product must be diluted before intravenous administration. The chemical name of ephedrine sulfate is (1R,2S)-(-)-2-methylamine-1-phenylpropan-1-ol sulfate (2:1) (salt). Its molecular weight is 428.54. The structural formula is. Image 1. Ephedrine sulfate darkens on exposure to light. It is freely soluble in water and ethanol, very slightly soluble in chloroform, and practically insoluble in ether."
},
{
"NDCCode": "43742-0001-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0001-1)",
"NDC11Code": "43742-0001-01",
"ProductNDC": "43742-0001",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Rheumatism",
"NonProprietaryName": "Benzoicum Acidum, Pulsatilla, Rhododendron Chrysanthum, Spiraea Ulmaria, Aconitum Napellus, Dulcamara, Euphorbium Officinarum, Ledum Palustre, Asclepias Tuberosa, Lithium Benzoicum,",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120405",
"EndMarketingDate": "20200925",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "BENZOIC ACID; PULSATILLA VULGARIS; RHODODENDRON AUREUM LEAF; FILIPENDULA ULMARIA ROOT; ACONITUM NAPELLUS; SOLANUM DULCAMARA FLOWER; EUPHORBIA RESINIFERA RESIN; LEDUM PALUSTRE TWIG; ASCLEPIAS TUBEROSA ROOT; LITHIUM BENZOATE",
"StrengthNumber": "3; 3; 3; 3; 4; 4; 4; 4; 6; 8",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2020-09-26",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0005-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0005-1)",
"NDC11Code": "43742-0005-01",
"ProductNDC": "43742-0005",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "B Complex Mix",
"NonProprietaryName": "Magnesium Oroticum, Beta Vulgaris, Ascorbicum Acidum, Citricum Acidum, Cysteinum, Pulsatilla, Adenine, Amygdalin, Atp, Cholinum, Cyanocopalamin, Folic Acid, Insotil, Niacin, P-aminobenzoic Acid, Pangamic Acid, Panthothenic Acid,",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120416",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "MAGNESIUM OROTATE; BETA VULGARIS; ASCORBIC ACID; ANHYDROUS CITRIC ACID; CYSTEINE; PULSATILLA VULGARIS; ADENINE; AMYGDALIN; ADENOSINE TRIPHOSPHATE; CHOLINE HYDROXIDE; CYANOCOBALAMIN; FOLIC ACID; INOSITOL; NIACIN; AMINOBENZOIC ACID; PANGAMIC ACID; PANTOTHENIC ACID; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SULFUR; THIAMINE; SODIUM DIETHYL OXALACETATE; OROTIC ACID MONOHYDRATE; MANGANESE PHOSPHATE, DIBASIC; ESCHERICHIA COLI; PROTEUS MORGANII",
"StrengthNumber": "12; 2; 3; 4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 7; 8; 10; 30; 30",
"StrengthUnit": "[hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL",
"Status": "Deprecated",
"LastUpdate": "2018-10-30",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20181231"
},
{
"NDCCode": "43742-0006-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0006-1)",
"NDC11Code": "43742-0006-01",
"ProductNDC": "43742-0006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Insect Bite",
"NonProprietaryName": "Hypericum Perforatum, Ledum Palustre, Latrodectus Mactans, Loxosceles Reclusa, Tarentula Cubensis, Tarentula Hispana, Lachesis Mutus, Lycopus Virginicus, Theridion, Cimex Lectularius, Formica Rufa, Pulex Irritans, Vespa Crabro",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20110926",
"EndMarketingDate": "20200915",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc",
"SubstanceName": "HYPERICUM PERFORATUM; LEDUM PALUSTRE TWIG; LATRODECTUS MACTANS; CITHARACANTHUS SPINICRUS; LYCOSA TARANTULA; LACHESIS MUTA VENOM; LYCOPUS VIRGINICUS; THERIDION CURASSAVICUM; CIMEX LECTULARIUS; FORMICA RUFA; PULEX IRRITANS; VESPA CRABRO; LOXOSCELES RECLUSA",
"StrengthNumber": "3; 4; 8; 8; 8; 10; 12; 12; 15; 15; 15; 15; 12",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL",
"Status": "Deprecated",
"LastUpdate": "2020-09-16",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0008-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0008-1)",
"NDC11Code": "43742-0008-01",
"ProductNDC": "43742-0008",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Heart Fatigue",
"NonProprietaryName": "Spigelia Anthelmia, Kali Carbonicum, Arnica Montana, Cactus Grandiflorus, Gelsemium Sempervirens, Castoreum, Glonoinum, Ranunculus Bulbosus, Heart (suis), Abrotanum, Sulphur",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120418",
"EndMarketingDate": "20210422",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "SPIGELIA ANTHELMIA; POTASSIUM CARBONATE; ARNICA MONTANA; SELENICEREUS GRANDIFLORUS STEM; GELSEMIUM SEMPERVIRENS ROOT; CASTOR CANADENSIS SCENT GLAND SECRETION; NITROGLYCERIN; RANUNCULUS BULBOSUS; PORK HEART; ARTEMISIA ABROTANUM FLOWERING TOP; SULFUR",
"StrengthNumber": "2; 3; 4; 4; 4; 6; 6; 6; 8; 12; 12",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2021-04-23",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0011-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0011-1)",
"NDC11Code": "43742-0011-01",
"ProductNDC": "43742-0011",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Lymph Spleen Combo",
"NonProprietaryName": "Castanea Vesca, Juniperus Communis, Phytolacca Decandra, Quercus Glandium Spiritus, Myosotis Arvensis, Natrum Sulphuricum, Ceanothus Americanus, Helianthus Annuus, Natrum Muriaticum, Lymph (suis), Spleen (suis), Thymus (suis),",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120501",
"EndMarketingDate": "20180806",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "CASTANEA SATIVA LEAF; JUNIPER BERRY; PHYTOLACCA AMERICANA ROOT; QUERCUS ROBUR NUT; MYOSOTIS ARVENSIS; SODIUM SULFATE; CEANOTHUS AMERICANUS LEAF; HELIANTHUS ANNUUS FLOWERING TOP; SODIUM CHLORIDE; SUS SCROFA LYMPH; SUS SCROFA SPLEEN; SUS SCROFA THYMUS; QUININE ARSENATE; ADENOSINE TRIPHOSPHATE; UBIDECARENONE; IRON; AMBER; APIS MELLIFERA",
"StrengthNumber": "3; 3; 3; 4; 6; 6; 6; 6; 6; 8; 8; 8; 8; 12; 12; 30; 30; 200",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL",
"Status": "Deprecated",
"LastUpdate": "2018-08-06",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0013-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0013-1)",
"NDC11Code": "43742-0013-01",
"ProductNDC": "43742-0013",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Celeragesic",
"NonProprietaryName": "Cchinacea, Echinacea Purpurea, Hamamelis Virginiana, Bellis Perennis, Calendula Officinalis, Aconitum Napellus, Chamomilla, Hypericum Perforatum, Belladonna, Millefolium, Bryonia, Rhus Toxicodendron, Atp, Coenzyme A,",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120430",
"EndMarketingDate": "20180702",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "ECHINACEA, UNSPECIFIED; ECHINACEA PURPUREA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; BELLIS PERENNIS; CALENDULA OFFICINALIS FLOWERING TOP; ACONITUM NAPELLUS; MATRICARIA RECUTITA; HYPERICUM PERFORATUM; ATROPA BELLADONNA; ACHILLEA MILLEFOLIUM; BRYONIA ALBA ROOT; ARNICA MONTANA; TOXICODENDRON PUBESCENS LEAF; ADENOSINE TRIPHOSPHATE; COENZYME A; CALCIUM SULFIDE; MERCURIUS SOLUBILIS; NADIDE; ORNITHOGALUM UMBELLATUM; HELIANTHEMUM NUMMULARIUM FLOWER; IMPATIENS GLANDULIFERA FLOWER; PRUNUS CERASIFERA FLOWER; CLEMATIS VITALBA FLOWER; LACTIC ACID, L-; COMFREY ROOT; ACTIVATED CHARCOAL; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; SUS SCROFA THALAMUS; PROTEUS MORGANII; UBIDECARENONE",
"StrengthNumber": "2; 2; 2; 2; 2; 3; 3; 3; 3; 3; 4; 4; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 12; 12; 12; 12; 30; 8",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2018-07-02",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0030-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0030-1)",
"NDC11Code": "43742-0030-01",
"ProductNDC": "43742-0030",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Matrix Support",
"NonProprietaryName": "Ceanothus Americanus, Hydrastis Canadensis, Veratrum Album, Anacardium Orientale, Argentum Nitricum, Condurango, Momordica Balsamina, Oxalis Acetosella, Pulsatilla, Bile Duct (suis), Colon (suis), Duodenum (suis), Esophagus (suis), Eye (suis), Gallbladder (suis), Ileum (suis), Intestine (suis), Ipecacuanha, Jejunum (suis), Kali Bichromicum, Lung (suis), Mucosa Nasalis Suis, Natrum Oxalaceticum, Oral Mucosa (suis), Pancreas Suis, Phosphorus, Rectum (suis), Stomach (suis), Sulphur, Mannan",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120514",
"EndMarketingDate": "20200915",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "CEANOTHUS AMERICANUS LEAF; GOLDENSEAL; VERATRUM ALBUM ROOT; SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; MARSDENIA CONDURANGO BARK; MOMORDICA BALSAMINA IMMATURE FRUIT; OXALIS ACETOSELLA LEAF; PULSATILLA VULGARIS; SUS SCROFA BILE DUCT; SUS SCROFA COLON; SUS SCROFA DUODENUM; SUS SCROFA ESOPHAGUS; SUS SCROFA EYE; SUS SCROFA GALLBLADDER; SUS SCROFA ILEUM; PORK INTESTINE; IPECAC; SUS SCROFA JEJUNUM; POTASSIUM DICHROMATE; SUS SCROFA LUNG; SUS SCROFA NASAL MUCOSA; SODIUM DIETHYL OXALACETATE; SUS SCROFA ORAL MUCOSA; SUS SCROFA PANCREAS; PHOSPHORUS; SUS SCROFA RECTUM; SUS SCROFA STOMACH; SULFUR; YEAST MANNAN; ATROPA BELLADONNA; WOOD CREOSOTE; LACHESIS MUTA VENOM; MANDRAGORA OFFICINARUM ROOT; SUS SCROFA URINARY BLADDER; SHIGELLA DYSENTERIAE",
"StrengthNumber": "4; 4; 4; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 10; 10; 10; 10; 6; 30",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL",
"Status": "Deprecated",
"LastUpdate": "2020-09-16",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0050-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0050-1)",
"NDC11Code": "43742-0050-01",
"ProductNDC": "43742-0050",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Circulation",
"NonProprietaryName": "Cactus Grandiflorus, Kali Carbonicum, Kalmia Latifolia, Arnica Montana, Glonoinum, Ignatia Amara, Lacticum Acidum, Ranunculus Bulbosus, Alpha-ketoglutaricum Acidum, Arsenicum Album, Cor (suis), Fumaricum Acidum, Hepar Suis, Malic Acid, Natrum Oxalaceticum, Phosphorus, Strophanthus Hispidus, Spigelia Anthelmia, Carbo Vegetabilis, Naja Tripudians, Cytomegalovirus, Epstein-barr Virus",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120601",
"EndMarketingDate": "20200918",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals",
"SubstanceName": "SELENICEREUS GRANDIFLORUS STEM; POTASSIUM CARBONATE; KALMIA LATIFOLIA LEAF; ARNICA MONTANA; NITROGLYCERIN; STRYCHNOS IGNATII SEED; LACTIC ACID, DL-; RANUNCULUS BULBOSUS; .ALPHA.-KETOGLUTARIC ACID; ARSENIC TRIOXIDE; PORK HEART; FUMARIC ACID; PORK LIVER; MALIC ACID; SODIUM DIETHYL OXALACETATE; PHOSPHORUS; STROPHANTHUS HISPIDUS SEED; SPIGELIA ANTHELMIA; ACTIVATED CHARCOAL; NAJA NAJA VENOM; HUMAN HERPESVIRUS 5; HUMAN HERPESVIRUS 4",
"StrengthNumber": "3; 4; 4; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 10; 12; 15; 17; 17",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2020-09-19",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0053-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0053-1)",
"NDC11Code": "43742-0053-01",
"ProductNDC": "43742-0053",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Spine And Nerve Balance Core Formula",
"NonProprietaryName": "Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Cuprum Aceticum, Nadidum, Natrum Oxalaceticum, Nicotinamidum, Picricum Acidum Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (suis), Silicea, Argentum Metallicum, Calcarea Phosphorica, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20140306",
"EndMarketingDate": "20200930",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals Inc.",
"SubstanceName": "BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; LEDUM PALUSTRE TWIG; RANUNCULUS BULBOSUS; HORSE CHESTNUT; CUPRIC ACETATE; NADIDE; SODIUM DIETHYL OXALACETATE; NIACINAMIDE; PICRIC ACID; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE; .ALPHA.-LIPOIC ACID; AMMONIUM CHLORIDE; SUS SCROFA CARTILAGE; SUS SCROFA INTERVERTEBRAL DISC; SILICON DIOXIDE; SILVER; TRIBASIC CALCIUM PHOSPHATE; COENZYME A; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; PSEUDOGNAPHALIUM OBTUSIFOLIUM; SUS SCROFA BONE MARROW; MERCURIC OXIDE; SULFUR; ENTEROBACTER CLOACAE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; PROTEUS MORGANII; PROTEUS VULGARIS",
"StrengthNumber": "4; 4; 4; 4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 10; 10; 10; 10; 10; 10; 10; 10; 28; 30; 30; 30; 30",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL",
"Status": "Deprecated",
"LastUpdate": "2020-10-01",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0056-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0056-1)",
"NDC11Code": "43742-0056-01",
"ProductNDC": "43742-0056",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Post-dental Visit",
"NonProprietaryName": "Chamomilla, Echinacea, Hamamelis Virginiana, Hypericum Perforatum, Millefolium, Bryonia, Calendula Officinalis, Arnica Montana, Belladonna, Bellis Perennis, Rhus Toxicodendron, Hepar Sulphuris Calcareum, Star Of Bethleham, Rock Rose, Impatiens, Cherry Plum, Clematis, Carbo Vegetabilis",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120618",
"EndMarketingDate": "20190114",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "MATRICARIA RECUTITA; ECHINACEA, UNSPECIFIED; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HYPERICUM PERFORATUM; ACHILLEA MILLEFOLIUM; BRYONIA ALBA ROOT; CALENDULA OFFICINALIS FLOWERING TOP; ARNICA MONTANA; ATROPA BELLADONNA; BELLIS PERENNIS; TOXICODENDRON PUBESCENS LEAF; CALCIUM SULFIDE; ORNITHOGALUM UMBELLATUM; HELIANTHEMUM NUMMULARIUM FLOWER; IMPATIENS GLANDULIFERA FLOWER; PRUNUS CERASIFERA FLOWER; CLEMATIS VITALBA FLOWER; ACTIVATED CHARCOAL",
"StrengthNumber": "3; 3; 3; 3; 3; 4; 4; 4; 6; 6; 6; 8; 8; 8; 8; 8; 8; 12",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2019-01-14",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0060-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0060-1) ",
"NDC11Code": "43742-0060-01",
"ProductNDC": "43742-0060",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Thyroplus",
"NonProprietaryName": "Fucus Vesiculosus, Spongia Tosta, Phosphoricum Acidum, Pituitary (suis), Thyroidinum (suis), Calcarea Carbonica, Iodium, Iridium Metallicum",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120626",
"EndMarketingDate": "20201110",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "FUCUS VESICULOSUS; SPONGIA OFFICINALIS SKELETON, ROASTED; PHOSPHORIC ACID; SUS SCROFA PITUITARY GLAND; THYROID, PORCINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; IODINE; IRIDIUM",
"StrengthNumber": "3; 4; 6; 8; 8; 12; 12; 12",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2020-11-11",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20120626",
"EndMarketingDatePackage": "20201110",
"SamplePackage": "N"
},
{
"NDCCode": "43742-0061-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0061-1)",
"NDC11Code": "43742-0061-01",
"ProductNDC": "43742-0061",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Detox",
"ProprietaryNameSuffix": "I",
"NonProprietaryName": "Carduus Marianus, Chelidonium Majus, Cinchona Officinalis, Lycopodium Clavatum, Taraxacum Officinale, Veratrum Album, Avena Sativa, Cynara Scolymus, Methylcobalamin, Menadione, Alpha-lipoicum Acidum, Hepar Suis, Colon (suis), Duodenum (suis), Gallbladder (suis), Intestine (suis), Lymph Node (suis), Pancreas Suis, Thymus (suis), Alpha-ketoglutaricum Acidum, Cholesterinum, Formicum Acidum, Glyoxal Trimer Dihydrate, Histaminum Hydrochloricum, Malic Acid, Natrum Oxalaceticum, Sulphur",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120629",
"EndMarketingDate": "20200925",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "SILYBUM MARIANUM SEED; CHELIDONIUM MAJUS; CINCHONA OFFICINALIS BARK; LYCOPODIUM CLAVATUM SPORE; TARAXACUM OFFICINALE; VERATRUM ALBUM ROOT; AVENA SATIVA FLOWERING TOP; CYNARA SCOLYMUS LEAF; METHYLCOBALAMIN; MENADIONE; .ALPHA.-LIPOIC ACID; PORK LIVER; SUS SCROFA COLON; SUS SCROFA DUODENUM; SUS SCROFA GALLBLADDER; PORK INTESTINE; SUS SCROFA LYMPH; SUS SCROFA PANCREAS; SUS SCROFA THYMUS; .ALPHA.-KETOGLUTARIC ACID; CHOLESTEROL; FORMIC ACID; GLYOXAL TRIMER DIHYDRATE; HISTAMINE DIHYDROCHLORIDE; MALIC ACID; SODIUM DIETHYL OXALACETATE; SULFUR; OYSTER SHELL CALCIUM CARBONATE, CRUDE; OROTIC ACID MONOHYDRATE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; PROTEUS MORGANII",
"StrengthNumber": "3; 4; 4; 4; 4; 4; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 10; 10; 10; 10; 10; 10; 10; 13; 28; 7; 30; 30",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL",
"Status": "Deprecated",
"LastUpdate": "2020-09-26",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0062-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0062-1)",
"NDC11Code": "43742-0062-01",
"ProductNDC": "43742-0062",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Detox",
"ProprietaryNameSuffix": "Iii",
"NonProprietaryName": "Conium Maculatum, Dulcamara, Echinacea, Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbicum Acidum, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Lymph (suis), Sulphur, Glandula Suprarenalis Suis, Phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus (suis), Spleen (suis) Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Funiculus Umbilicalis Suis, Tonsil (suis), Gaertner Bach, Triiodothyronine, Medulla Ossis Suis, Mutabile Bach",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120628",
"EndMarketingDate": "20171003",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "CONIUM MACULATUM FLOWERING TOP; SOLANUM DULCAMARA TOP; ECHINACEA, UNSPECIFIED; HORSE CHESTNUT; ANTIMONY POTASSIUM TARTRATE; ASCORBIC ACID; PROTORTONIA CACTI; GALIUM APARINE; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; PULSATILLA VULGARIS; LACTIC ACID, L-; SUS SCROFA LYMPH; SULFUR; SUS SCROFA ADRENAL GLAND; PHENYLALANINE; TRIBASIC CALCIUM PHOSPHATE; FERROSOFERRIC PHOSPHATE; PORK LIVER; SUS SCROFA HYPOTHALAMUS; SUS SCROFA SPLEEN; CORTISONE ACETATE; MERCURIUS SOLUBILIS; BARIUM CARBONATE; SUS SCROFA UMBILICAL CORD; SUS SCROFA TONSIL; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; LIOTHYRONINE; SUS SCROFA BONE MARROW; ESCHERICHIA COLI",
"StrengthNumber": "4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 10; 10; 10; 10; 10; 13; 13; 28; 6; 6; 9; 10; 12; 30",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL",
"Status": "Deprecated",
"LastUpdate": "2017-10-05"
},
{
"NDCCode": "43742-0072-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0072-1)",
"NDC11Code": "43742-0072-01",
"ProductNDC": "43742-0072",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Spinalmax",
"NonProprietaryName": "Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Cuprum Aceticum, Nadidum, Natrum Oxalaceticum, Nicotinamidum, Picricum Acidum, Pyridoxinum, Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (suis), Silicea, Argentum Metallicum, Calcarea Phosphorica, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20140402",
"EndMarketingDate": "20200913",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; LEDUM PALUSTRE TWIG; RANUNCULUS BULBOSUS; HORSE CHESTNUT; CUPRIC ACETATE; NADIDE; SODIUM DIETHYL OXALACETATE; NIACINAMIDE; PICRIC ACID; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE; .ALPHA.-LIPOIC ACID; AMMONIUM CHLORIDE; SUS SCROFA CARTILAGE; SUS SCROFA INTERVERTEBRAL DISC; SILICON DIOXIDE; SILVER; TRIBASIC CALCIUM PHOSPHATE; COENZYME A; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; PSEUDOGNAPHALIUM OBTUSIFOLIUM; SUS SCROFA BONE MARROW; MERCURIC OXIDE; SULFUR; ENTEROBACTER CLOACAE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; PROTEUS MORGANII; PROTEUS VULGARIS",
"StrengthNumber": "4; 4; 4; 4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 10; 10; 10; 10; 10; 10; 10; 10; 28; 30; 30; 30; 30",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL",
"Status": "Deprecated",
"LastUpdate": "2020-09-15",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0073-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0073-1) ",
"NDC11Code": "43742-0073-01",
"ProductNDC": "43742-0073",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Detox",
"ProprietaryNameSuffix": "Ii",
"NonProprietaryName": "Solidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, Equisetum Hyemale, Argentum Nitricum 6x, Cantharis, Capsicum Annuum, Cuprum Sulphuricum, Orthosiphon Stamineus, Pareira Brava, Sarsaparilla, Terebinthina, Apis Venenum Purum, Barosma, Mercurius Corrosivus, Pyelon (suis), Ureter (suis), Urethra (suis), Urinary Bladder (suis), Glyoxal Trimer Dihydrate, Hepar Sulphuris Calcareum, Natrum Pyruvicum, Quercetin, Colibacillinum Cum Natrum Muriaticum, Dysentery Bacillus",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120710",
"EndMarketingDate": "20200805",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "SOLIDAGO VIRGAUREA FLOWERING TOP; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; EQUISETUM HYEMALE; SILVER NITRATE; LYTTA VESICATORIA; CAPSICUM; CUPRIC SULFATE; CLERODENDRANTHUS SPICATUS LEAF; CHONDRODENDRON TOMENTOSUM ROOT; SMILAX ORNATA ROOT; TURPENTINE OIL; APIS MELLIFERA VENOM; AGATHOSMA BETULINA LEAF; MERCURIC CHLORIDE; SUS SCROFA RENAL PELVIS; SUS SCROFA URETER; SUS SCROFA URETHRA; SUS SCROFA URINARY BLADDER; GLYOXAL TRIMER DIHYDRATE; CALCIUM SULFIDE; SODIUM PYRUVATE; QUERCETIN; ESCHERICHIA COLI; SHIGELLA DYSENTERIAE",
"StrengthNumber": "3; 4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 10; 10; 10; 10; 15; 30",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL",
"Status": "Deprecated",
"LastUpdate": "2020-08-06",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20120710",
"EndMarketingDatePackage": "20200805",
"SamplePackage": "N"
},
{
"NDCCode": "43742-0087-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0087-1)",
"NDC11Code": "43742-0087-01",
"ProductNDC": "43742-0087",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Intestinal Distress",
"NonProprietaryName": "Echinacea, Colchicum Autumnale, Aloe Socotrina, Colocynthis, Mercurius Corrosivus, Nux Vomica, Arsenicum Album",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120821",
"EndMarketingDate": "20171015",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "ECHINACEA ANGUSTIFOLIA; COLCHICUM AUTUMNALE BULB; ALOE; CITRULLUS COLOCYNTHIS FRUIT PULP; MERCURIC CHLORIDE; STRYCHNOS NUX-VOMICA SEED; ARSENIC TRIOXIDE; QUININE SULFATE; VIBRIO CHOLERAE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; CAMPYLOBACTER JEJUNI; ESCHERICHIA COLI; HELICOBACTER PYLORI; SHIGELLA DYSENTERIAE; YERSINIA ENTEROCOLITICA; BOTULINUM TOXIN TYPE A; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI",
"StrengthNumber": "3; 4; 6; 6; 6; 6; 6; 12; 12; 15; 30; 30; 30; 30; 30; 30; 33",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2017-10-19"
},
{
"NDCCode": "43742-0090-1",
"PackageDescription": "60 mL in 1 BOTTLE, DROPPER (43742-0090-1)",
"NDC11Code": "43742-0090-01",
"ProductNDC": "43742-0090",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Lymph Drainage",
"NonProprietaryName": "Citrus Limonum, Echinacea, Scrophularia Nodosa, Teucrium Scorodonia, Baptisia Tinctoria, Lobelia Inflata, Phytolacca Decandra",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120821",
"EndMarketingDate": "20171108",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "LEMON JUICE; ECHINACEA, UNSPECIFIED; SCROPHULARIA NODOSA; TEUCRIUM SCORODONIA FLOWERING TOP; BAPTISIA TINCTORIA; LOBELIA INFLATA; PHYTOLACCA AMERICANA ROOT; PINUS SYLVESTRIS LEAFY TWIG; ZINC GLUCONATE; THUJA OCCIDENTALIS LEAFY TWIG; CAPSICUM; COPPER GLUCONATE; MAGNESIUM GLUCONATE; ARANEUS DIADEMATUS; ARSENIC TRIIODIDE; CENTAURIUM ERYTHRAEA; CARPINUS BETULUS FLOWER; LARIX DECIDUA FLOWERING TOP; SUS SCROFA LYMPH; SUS SCROFA SPLEEN; SUS SCROFA THYMUS; LACHESIS MUTA VENOM",
"StrengthNumber": "1; 1; 1; 1; 1; 3; 3; 3; 3; 4; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 12",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2017-11-08"
},
{
"NDCCode": "43742-0111-1",
"PackageDescription": "960 mL in 1 PACKAGE (43742-0111-1)",
"NDC11Code": "43742-0111-01",
"ProductNDC": "43742-0111",
"ProductTypeName": "BULK INGREDIENT",
"NonProprietaryName": "Astragalus Membranaceus, Baptisia Tinctoria, Condurango, Echinacea (angustifolia), Hydrastis Canadensis, Nasturtium Aquaticum, Osha, Phytolacca Decandra, Propolis, Thymus (suis), Aranea Diadema, Gelsemium Sempervirens, Iodium, Ipecacuanha, Lycopodium Clavatum, Mercurius Solubilis, Muriaticum Acidum, Nitricum Acidum, Rhus Tox, Silicea Tabebuia Impetiginosa, Epstein-barr Virus Nosode",
"DosageFormName": "LIQUID",
"StartMarketingDate": "20140904",
"EndMarketingDate": "20191114",
"MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
"LabelerName": "Deseret Biologicals",
"SubstanceName": "ASTRAGALUS PROPINQUUS ROOT; BAPTISIA TINCTORIA ROOT; MARSDENIA CONDURANGO BARK; ECHINACEA, UNSPECIFIED; GOLDENSEAL; NASTURTIUM OFFICINALE; LIGUSTICUM PORTERI ROOT; PHYTOLACCA AMERICANA ROOT; PROPOLIS WAX; SUS SCROFA THYMUS; ARANEUS DIADEMATUS; GELSEMIUM SEMPERVIRENS ROOT; IODINE; IPECAC; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; HYDROCHLORIC ACID; NITRIC ACID; TOXICODENDRON PUBESCENS LEAF; SILICON DIOXIDE; TABEBUIA IMPETIGINOSA BARK; HUMAN HERPESVIRUS 4",
"StrengthNumber": "6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 30",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2014-02-04",
"ListingRecordCertifiedThrough": "20181231"
},
{
"NDCCode": "43742-0126-1",
"PackageDescription": "960 mL in 1 BOTTLE (43742-0126-1)",
"NDC11Code": "43742-0126-01",
"ProductNDC": "43742-0126",
"ProductTypeName": "DRUG FOR FURTHER PROCESSING",
"NonProprietaryName": "Echinacea (angustifolia), Hydrastis Canadensis, Nasturtium Aquaticum, Thuja Occidentalis, Thymus (suis), Belladonna, Eupatorium Perfoliatum, Gelsemium Sempervirens, Iodium, Lachesis Mutus, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Selenium Metallicum, Zincum Metallicum, Cytomegalovirus Nosode, Herpes Simplex 1 Nosode, Herpes Simplex 2 Nosode, Herpes Zoster Nosode, Poliomyelitis Nosode, Epstein Barr Virus Nosode, Morbillinum, Parotidinum, Rubella Nosode, Pyrogenium",
"DosageFormName": "LIQUID",
"StartMarketingDate": "20120829",
"EndMarketingDate": "20220427",
"MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; NASTURTIUM OFFICINALE; THUJA OCCIDENTALIS LEAFY TWIG; SUS SCROFA THYMUS; ATROPA BELLADONNA; EUPATORIUM PERFOLIATUM FLOWERING TOP; GELSEMIUM SEMPERVIRENS ROOT; IODINE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORIC ACID; PHOSPHORUS; SELENIUM; ZINC; HUMAN HERPESVIRUS 5; HUMAN HERPESVIRUS 1; HUMAN HERPESVIRUS 2; HUMAN HERPESVIRUS 3; POLIOVIRUS; HUMAN HERPESVIRUS 4; MEASLES VIRUS; MUMPS VIRUS; RUBELLA VIRUS; RANCID BEEF; HEPATITIS B VIRUS; HUMAN COXSACKIEVIRUS B1; HUMAN COXSACKIEVIRUS B4; ANTIMONY TRISULFIDE; LEDUM PALUSTRE TWIG; THIMEROSAL",
"StrengthNumber": "6; 6; 6; 6; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 15; 15; 15; 15; 18; 30; 30; 30; 30; 33; 8; 8; 30; 30; 30",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL",
"Status": "Deprecated",
"LastUpdate": "2014-02-04"
},
{
"NDCCode": "43742-0130-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0130-1)",
"NDC11Code": "43742-0130-01",
"ProductNDC": "43742-0130",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Sinusitis",
"NonProprietaryName": "Pulsatilla, Plantago Major, Euphorbium Officinarum, Luffa Operculata, Mercurius Iodatus Ruber, Mucosa Nasalis Suis, Argentum Nitricum",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120906",
"EndMarketingDate": "20180905",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "PULSATILLA VULGARIS; PLANTAGO MAJOR; EUPHORBIA RESINIFERA RESIN; LUFFA OPERCULATA FRUIT; MERCURIC IODIDE; SUS SCROFA NASAL MUCOSA; SILVER NITRATE; CALCIUM SULFIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM CHLORIDE; SINUSITISINUM",
"StrengthNumber": "2; 3; 4; 6; 8; 8; 10; 10; 12; 12; 18",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2018-09-07",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "43742-0131-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0131-1) ",
"NDC11Code": "43742-0131-01",
"ProductNDC": "43742-0131",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Tobacco",
"NonProprietaryName": "Avena Sativa, Lobelia Inflata, Cactus Grandiflorus, Tabacum, Gelsemium Sempervirens, Selenium Metallicum, Staphysagria, Vanadium Metallicum",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120920",
"EndMarketingDate": "20220713",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "AVENA SATIVA FLOWERING TOP; DELPHINIUM STAPHISAGRIA SEED; GELSEMIUM SEMPERVIRENS ROOT; LOBELIA INFLATA; SELENICEREUS GRANDIFLORUS STEM; SELENIUM; TOBACCO LEAF; VANADIUM",
"StrengthNumber": "1; 12; 12; 3; 4; 12; 6; 12",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Pharm_Classes": "Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]",
"Status": "Deprecated",
"LastUpdate": "2022-07-14",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20170605",
"EndMarketingDatePackage": "20220713",
"SamplePackage": "N"
},
{
"NDCCode": "43742-0132-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (43742-0132-1)",
"NDC11Code": "43742-0132-01",
"ProductNDC": "43742-0132",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Ebv",
"NonProprietaryName": "Baptisia Tinctoria, Condurango, Echinacea, Hydrastis Canadensis, Nasturtium Aquaticum, Osha, Phytolacca Decandra, Tabebuia Impetiginosa, Astragalus Menziesii, Propolis, Glandula Suprarenalis Suis, Thymus (suis), Aranea Diadema, Gelsemium Sempervirens, Ipecacuanha, Lycopodium Clavatum, Mercurius Solubilis, Muriaticum Acidum, Nitricum Acidum, Rhus Toxicodendron, Selenium Metallicum, Silicea, Epstein Barr Virus",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20120910",
"EndMarketingDate": "20180928",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Deseret Biologicals, Inc.",
"SubstanceName": "BAPTISIA TINCTORIA; MARSDENIA CONDURANGO BARK; ECHINACEA, UNSPECIFIED; GOLDENSEAL; NASTURTIUM AQUATICUM; LIGUSTICUM PORTERI ROOT; PHYTOLACCA AMERICANA ROOT; TABEBUIA IMPETIGINOSA BARK; ASTRAGALUS NUTTALLII LEAF; PROPOLIS WAX; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYMUS; ARANEUS DIADEMATUS; GELSEMIUM SEMPERVIRENS ROOT; IPECAC; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; HYDROCHLORIC ACID; NITRIC ACID; TOXICODENDRON PUBESCENS LEAF; SELENIUM; SILICON DIOXIDE; HUMAN HERPESVIRUS 4",
"StrengthNumber": "3; 3; 3; 3; 3; 3; 3; 3; 6; 6; 8; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 30",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2018-09-29",
"ProductNdcExcludeFlag": "N"
}
]
}
{"NDC":[{"NDCCode":"43742-1325-4","ProprietaryName":"Rheumagesic","NonProprietaryName":"Arnica Montana, Apis Mellifica, Benzoicum Acidum, Cartilago Suis, Ledum Palustre, Pantothenic Acid, Ruta Graveolens, Rhododendron Chrysanthum, Causticum, Formica Rufa, Sepia, Alpha-lipoicum Acidum, Aurum Metallicum, Calcarea Phosphorica, Colchicum Autumnale, Phytolacca Decandra, Radium Bromatum, Rhus Venenata, Thuja Occidentalis, Lac Caninum"},{"NDCCode":"43742-0702-4","NonProprietaryName":"Aconitum Napellus, Antimonium Tartaricum, Arsenicum Iodatum, Belladonna, Bryonia, Causticum, Coccus Cacti, Cuprum Aceticum, Drosera (rotundifolia), Hyoscyamus Niger, Ipecacuanha, Kreosotum, Lobelia Inflata, Phosphorus, Scilla Maritima, Sticta Pulmonaria, Silicea, Carbo Vegetabilis, Kali Carbonicum, Lachesis Mutus, Pertussinum, Tetanus Toxin"},{"NDCCode":"22840-1325-4","ProprietaryName":"Firebush Kochia","NonProprietaryName":"Kochia Scoparia"},{"NDCCode":"36987-1325-4","ProprietaryName":"Fig","NonProprietaryName":"Fig"},{"NDCCode":"70771-1325-4","ProprietaryName":"Candesartan Cilexetil And Hydrochlorothiazide","NonProprietaryName":"Candesartan Cilexetil And Hydrochlorothiazide"},{"NDCCode":"71335-1325-4","ProprietaryName":"Hydroxyzine Pamoate","NonProprietaryName":"Hydroxyzine Pamoate"},{"NDCCode":"0115-1325-10","ProprietaryName":"Fenofibric Acid","NonProprietaryName":"Fenofibric Acid"},{"NDCCode":"51662-1325-1","ProprietaryName":"Ephedrine Sulfate","NonProprietaryName":"Ephedrine Sulfate"},{"NDCCode":"43742-0001-1","ProprietaryName":"Rheumatism","NonProprietaryName":"Benzoicum Acidum, Pulsatilla, Rhododendron Chrysanthum, Spiraea Ulmaria, Aconitum Napellus, Dulcamara, Euphorbium Officinarum, Ledum Palustre, Asclepias Tuberosa, Lithium Benzoicum,"},{"NDCCode":"43742-0005-1","ProprietaryName":"B Complex Mix","NonProprietaryName":"Magnesium Oroticum, Beta Vulgaris, Ascorbicum Acidum, Citricum Acidum, Cysteinum, Pulsatilla, Adenine, Amygdalin, Atp, Cholinum, Cyanocopalamin, Folic Acid, Insotil, Niacin, P-aminobenzoic Acid, Pangamic Acid, Panthothenic Acid,"},{"NDCCode":"43742-0006-1","ProprietaryName":"Insect Bite","NonProprietaryName":"Hypericum Perforatum, Ledum Palustre, Latrodectus Mactans, Loxosceles Reclusa, Tarentula Cubensis, Tarentula Hispana, Lachesis Mutus, Lycopus Virginicus, Theridion, Cimex Lectularius, Formica Rufa, Pulex Irritans, Vespa Crabro"},{"NDCCode":"43742-0008-1","ProprietaryName":"Heart Fatigue","NonProprietaryName":"Spigelia Anthelmia, Kali Carbonicum, Arnica Montana, Cactus Grandiflorus, Gelsemium Sempervirens, Castoreum, Glonoinum, Ranunculus Bulbosus, Heart (suis), Abrotanum, Sulphur"},{"NDCCode":"43742-0011-1","ProprietaryName":"Lymph Spleen Combo","NonProprietaryName":"Castanea Vesca, Juniperus Communis, Phytolacca Decandra, Quercus Glandium Spiritus, Myosotis Arvensis, Natrum Sulphuricum, Ceanothus Americanus, Helianthus Annuus, Natrum Muriaticum, Lymph (suis), 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<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-1325-4) </PackageDescription>
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<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Rheumagesic</ProprietaryName>
<NonProprietaryName>Arnica Montana, Apis Mellifica, Benzoicum Acidum, Cartilago Suis, Ledum Palustre, Pantothenic Acid, Ruta Graveolens, Rhododendron Chrysanthum, Causticum, Formica Rufa, Sepia, Alpha-lipoicum Acidum, Aurum Metallicum, Calcarea Phosphorica, Colchicum Autumnale, Phytolacca Decandra, Radium Bromatum, Rhus Venenata, Thuja Occidentalis, Lac Caninum</NonProprietaryName>
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<StartMarketingDate>20190109</StartMarketingDate>
<EndMarketingDate>20251008</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>APIS MELLIFERA; ARNICA MONTANA; BENZOIC ACID; CANIS LUPUS FAMILIARIS MILK; CAUSTICUM; COLCHICUM AUTUMNALE BULB; FORMICA RUFA; GOLD; PANTOTHENIC ACID; PHYTOLACCA AMERICANA ROOT; RADIUM BROMIDE; RHODODENDRON AUREUM LEAF; RHODODENDRON TOMENTOSUM LEAFY TWIG; RUTA GRAVEOLENS FLOWERING TOP; SEPIA OFFICINALIS JUICE; SUS SCROFA CARTILAGE; THIOCTIC ACID; THUJA OCCIDENTALIS LEAFY TWIG; TOXICODENDRON VERNIX LEAFY TWIG; TRIBASIC CALCIUM PHOSPHATE</SubstanceName>
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<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Allergens [CS], Allergens [CS], Ammonium Ion Binding Activity [MoA], Bee Venoms [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nitrogen Binding Agent [EPC], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2025-10-08</LastUpdate>
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<EndMarketingDatePackage>20251008</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For temporary relief of symptoms related to arthritis including swelling, joint pain, back pain, inflammation in joints and muscle pain. **. **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.</IndicationAndUsage>
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<NDC>
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<PackageDescription>960 mL in 1 BOTTLE (43742-0702-4)</PackageDescription>
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<ProductTypeName>DRUG FOR FURTHER PROCESSING</ProductTypeName>
<NonProprietaryName>Aconitum Napellus, Antimonium Tartaricum, Arsenicum Iodatum, Belladonna, Bryonia, Causticum, Coccus Cacti, Cuprum Aceticum, Drosera (rotundifolia), Hyoscyamus Niger, Ipecacuanha, Kreosotum, Lobelia Inflata, Phosphorus, Scilla Maritima, Sticta Pulmonaria, Silicea, Carbo Vegetabilis, Kali Carbonicum, Lachesis Mutus, Pertussinum, Tetanus Toxin</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<StartMarketingDate>20151230</StartMarketingDate>
<EndMarketingDate>20220123</EndMarketingDate>
<MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
<LabelerName>Deseret Biologicals</LabelerName>
<SubstanceName>ACONITUM NAPELLUS; ANTIMONY POTASSIUM TARTRATE; ARSENIC TRIIODIDE; ATROPA BELLADONNA; BRYONIA ALBA ROOT; CAUSTICUM; PROTORTONIA CACTI; CUPRIC ACETATE; DROSERA ROTUNDIFOLIA; HYOSCYAMUS NIGER; IPECAC; WOOD CREOSOTE; LOBELIA INFLATA; PHOSPHORUS; DRIMIA MARITIMA BULB; LOBARIA PULMONARIA; SILICON DIOXIDE; ACTIVATED CHARCOAL; POTASSIUM CARBONATE; LACHESIS MUTA VENOM; HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED; TETANUS TOXIN</SubstanceName>
<StrengthNumber>6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 12; 12; 12; 30; 32</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2014-02-04</LastUpdate>
<ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>22840-1325-4</NDCCode>
<PackageDescription>50 mL in 1 VIAL, MULTI-DOSE (22840-1325-4) </PackageDescription>
<NDC11Code>22840-1325-04</NDC11Code>
<ProductNDC>22840-1325</ProductNDC>
<ProductTypeName>NON-STANDARDIZED ALLERGENIC</ProductTypeName>
<ProprietaryName>Firebush Kochia</ProprietaryName>
<NonProprietaryName>Kochia Scoparia</NonProprietaryName>
<DosageFormName>SOLUTION</DosageFormName>
<RouteName>INTRADERMAL; PERCUTANEOUS; SUBCUTANEOUS</RouteName>
<StartMarketingDate>19810915</StartMarketingDate>
<MarketingCategoryName>BLA</MarketingCategoryName>
<ApplicationNumber>BLA101833</ApplicationNumber>
<LabelerName>Greer Laboratories, Inc.</LabelerName>
<SubstanceName>BASSIA SCOPARIA POLLEN</SubstanceName>
<StrengthNumber>.1</StrengthNumber>
<StrengthUnit>g/mL</StrengthUnit>
<Pharm_Classes>Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Pollen Allergenic Extract [EPC], Pollen [CS]</Pharm_Classes>
<Status>Active</Status>
<LastUpdate>2025-06-07</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>19810915</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>Non-Standardized Allergenic Extracts are indicated for. : 1 Skin test diagnosis of patients with a clinical history of allergies to one or more of the specific non-standardized allergens., 2 Immunotherapy for the reduction of allergen-induced allergic symptoms confirmed by appropriate positive skin tests or by in vitro testing for allergen-specific IgE antibodies. .</IndicationAndUsage>
<Description>Non-Standardized Allergenic Extracts are sterile solutions used for percutaneous testing, intradermal testing, or subcutaneous immunotherapy. Aqueous extracts contain the soluble extractants of the source material in water for injection, 0.5% sodium chloride, 0.54% sodium bicarbonate, and 0.4% phenol. Glycerinated extracts contain the soluable extractants of the source material in water for injection and 50% glycerin, 0.25% sodium chloride, 0.27% sodium bicarbonate, and 0.2% phenol. The pH of the extracts range from 6 to 9. Certain food extracts (Barley, Oat, Pineapple, Rye, Spinach, and Wheat), labeled “For Diagnostic Use Only”, contain 0.1% sodium formaldehyde sulfoxylate as an antioxidant. Source materials used in the manufacture of allergenic extracts are collected from natural sources or from laboratory cultures. Non-Standardized Allergenic Extracts appear as clear and colorless to dark brown solutions that should be free of particulate matter. Extracts are labeled either as weight-to-volume based on the weight of the source material to the volume of the extracting fluid, or as PNU/milliliter with one PNU representing 0.00001 mg of protein nitrogen per milliliter.</Description>
</NDC>
<NDC>
<NDCCode>36987-1325-4</NDCCode>
<PackageDescription>50 mL in 1 VIAL, MULTI-DOSE (36987-1325-4)</PackageDescription>
<NDC11Code>36987-1325-04</NDC11Code>
<ProductNDC>36987-1325</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Fig</ProprietaryName>
<NonProprietaryName>Fig</NonProprietaryName>
<DosageFormName>INJECTION, SOLUTION</DosageFormName>
<RouteName>INTRADERMAL; SUBCUTANEOUS</RouteName>
<StartMarketingDate>19720829</StartMarketingDate>
<MarketingCategoryName>BLA</MarketingCategoryName>
<ApplicationNumber>BLA102192</ApplicationNumber>
<LabelerName>Nelco Laboratories, Inc.</LabelerName>
<SubstanceName>FIG</SubstanceName>
<StrengthNumber>.1</StrengthNumber>
<StrengthUnit>g/mL</StrengthUnit>
<Pharm_Classes>Non-Standardized Food Allergenic Extract [EPC],Non-Standardized Plant Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [CS],Dietary Proteins [CS],Plant Proteins [CS],Fruit Proteins [EXT]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2019-09-21</LastUpdate>
<ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
<IndicationAndUsage>Allergenic extracts are indicated for use in diagnostic testing and as part of a treatment regime for allergic disease, as established by allergy history and skin test reactivity. Allergenic extracts are indicated for the treatment of allergen specific allergic disease for use as hyposensitization or immunotherapy when avoidance of specific allergens can not be attained. The use of allergenic extracts for therapeutic purpose has been established by well-controlled clinical studies. Allergenic extracts may be used as adjunctive therapy along with pharmacotherapy which includes antihistamines, corticosteroids, and cromoglycate, and avoidance measures. Allergenic extracts for therapeutic use should be given using only the allergen selection to which the patient is allergic, has a history of exposure and are likely to be exposed to again.</IndicationAndUsage>
<Description>Allergenic extracts are sterile solutions consisting of the extractable components from various biological sources including pollens, inhalants, molds, animal epidermals and insects. Aqueous extracts are prepared using cocas fluid containing NaCl 0.5%, NaHCO3 0.0275%, WFI, preservative 0.4% Phenol. Glycerinated allergenic extracts are prepared with cocas fluid and glycerin to produce a 50% (v/v) allergenic extract. Allergenic Extracts are supplied as concentrations designated as protein nitrogen units (PNU) or weight/volume (w/v) ratio. Standardized extracts are designated in Bioequivalent Allergy Units (BAU) or Allergy Units (AU). (See product insert for standardized extracts). For diagnostic purposes, allergenic extracts are to be administered by prick-puncture or intradermal routes. Allergenic extracts are administered subcutaneously for immunotherapy injections.</Description>
</NDC>
<NDC>
<NDCCode>70771-1325-4</NDCCode>
<PackageDescription>10 BLISTER PACK in 1 CARTON (70771-1325-4) / 10 TABLET in 1 BLISTER PACK (70771-1325-2) </PackageDescription>
<NDC11Code>70771-1325-04</NDC11Code>
<ProductNDC>70771-1325</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Candesartan Cilexetil And Hydrochlorothiazide</ProprietaryName>
<NonProprietaryName>Candesartan Cilexetil And Hydrochlorothiazide</NonProprietaryName>
<DosageFormName>TABLET</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20180414</StartMarketingDate>
<MarketingCategoryName>ANDA</MarketingCategoryName>
<ApplicationNumber>ANDA203466</ApplicationNumber>
<LabelerName>Zydus Lifesciences Limited</LabelerName>
<SubstanceName>CANDESARTAN CILEXETIL; HYDROCHLOROTHIAZIDE</SubstanceName>
<StrengthNumber>16; 12.5</StrengthNumber>
<StrengthUnit>mg/1; mg/1</StrengthUnit>
<Pharm_Classes>Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]</Pharm_Classes>
<Status>Active</Status>
<LastUpdate>2024-11-14</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20180414</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>71335-1325-4</NDCCode>
<PackageDescription>10 CAPSULE in 1 BOTTLE (71335-1325-4) </PackageDescription>
<NDC11Code>71335-1325-04</NDC11Code>
<ProductNDC>71335-1325</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Hydroxyzine Pamoate</ProprietaryName>
<NonProprietaryName>Hydroxyzine Pamoate</NonProprietaryName>
<DosageFormName>CAPSULE</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20130603</StartMarketingDate>
<MarketingCategoryName>ANDA</MarketingCategoryName>
<ApplicationNumber>ANDA201507</ApplicationNumber>
<LabelerName>Bryant Ranch Prepack</LabelerName>
<SubstanceName>HYDROXYZINE PAMOATE</SubstanceName>
<StrengthNumber>25</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Pharm_Classes>Antihistamine [EPC], Histamine Receptor Antagonists [MoA]</Pharm_Classes>
<Status>Active</Status>
<LastUpdate>2025-10-13</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20220919</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For symptomatic relief of anxiety and tension associated with psychoneurosis and as an adjunct in organic disease states in which anxiety is manifested. Useful in the management of pruritus due to allergic conditions such as chronic urticaria and atopic and contact dermatoses, and in histamine-mediated pruritus. As a sedative when used as premedication and following general anesthesia, Hydroxyzine may potentiate meperidine (Demerol®) and barbiturates, so their use in pre-anesthetic adjunctive therapy should be modified on an individual basis. Atropine and other belladonna alkaloids are not affected by the drug. Hydroxyzine is not known to interfere with the action of digitalis in any way and it may be used concurrently with this agent. The effectiveness of hydroxyzine as an antianxiety agent for long-term use, that is, more than 4 months, has not been assessed by systematic clinical studies. The physician should reassess periodically the usefulness of the drug for the individual patient.</IndicationAndUsage>
<Description>Hydroxyzine pamoate is a light yellow odorless powder, practically insoluble in water and methanol and freely soluble in dimethylformamide. It is chemically designated as (±)-2-[2-[4-(p-Chloro-α-phenylbenzyl)-1-piperazinyl]ethoxy]ethanol 4,4 -methylenebis[3-hydroxy-2-naphthoate] (1:1) and can be structurally represented as follows. Chemical Formula: C21H27ClN2O2.C23H16O6. Molecular Weight: 763.29. Inert ingredients for the capsule formulations are: hard gelatin capsules (which contain gelatin, titanium dioxide, FD&C Blue #1, FD&C Red #40, D&C Yellow #10), printing ink which contains shellac glaze ~45% (20% esterified) in Ethanol, iron oxide black, n-butyl alcohol, isopropyl alcohol, propylene glycol and ammonium hydroxide 28%); magnesium stearate, microcrystalline cellulose, pregelatinized starch, sodium lauryl sulfate, sodium starch glycolate.</Description>
</NDC>
<NDC>
<NDCCode>0115-1325-10</NDCCode>
<PackageDescription>90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1325-10) </PackageDescription>
<NDC11Code>00115-1325-10</NDC11Code>
<ProductNDC>0115-1325</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Fenofibric Acid</ProprietaryName>
<NonProprietaryName>Fenofibric Acid</NonProprietaryName>
<DosageFormName>CAPSULE, DELAYED RELEASE</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20240601</StartMarketingDate>
<MarketingCategoryName>ANDA</MarketingCategoryName>
<ApplicationNumber>ANDA200264</ApplicationNumber>
<LabelerName>Amneal Pharmaceuticals of New York LLC</LabelerName>
<SubstanceName>FENOFIBRIC ACID</SubstanceName>
<StrengthNumber>135</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Pharm_Classes>Peroxisome Proliferator Receptor alpha Agonist [EPC]</Pharm_Classes>
<Status>Active</Status>
<LastUpdate>2025-08-11</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20240601</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>Fenofibric acid delayed-release capsules are indicated as adjunctive therapy to diet: 1 to reduce triglyceride (TG) levels in adults with severe hypertriglyceridemia (TG greater than or equal to 500 mg/dL)., 2 to reduce elevated low-density lipoprotein cholesterol (LDL-C) in adults with primary hyperlipidemia when use of recommended LDL-C lowering therapy is not possible.</IndicationAndUsage>
<Description>Fenofibric acid is a peroxisome proliferator-activated receptor (PPAR) alpha agonist available as delayed-release capsules for oral administration. Each delayed-release capsule contains choline fenofibrate, equivalent to 45 mg or 135 mg of fenofibric acid. The chemical name for choline fenofibrate is ethanaminium, 2-hydroxy-N,N,N-trimethyl, 2-[4-(4-chlorobenzoyl)phenoxy]-2-methylpropanoate (1:1) with the following structural formula. The molecular formula is C22H28ClNO5 and the molecular weight is 421.91 g/mole. Choline fenofibrate is freely soluble in water and methanol. The melting point is approximately 210°C. Choline fenofibrate is a white to off-white powder, which is stable under ordinary conditions. Each delayed-release capsule contains enteric coated seeds comprised of choline fenofibrate and the following inactive ingredients: acetyltributyl citrate, ethylcellulose, hypromellose, hypromellose phthalate, microcrystalline cellulose, silicon dioxide, and talc. The capsule shell of the 45 mg capsule contains the following inactive ingredients: FD&C Red #40, FD&C yellow #5, FD&C Yellow #6, gelatin, and titanium dioxide. The capsule shell of the 135 mg capsule contains the following inactive ingredients: FD&C Blue #1, FD&C Red #3, FD&C Yellow #5, FD&C Yellow #6, gelatin and titanium dioxide. The capsule is imprinted with black pharmaceutical ink which includes butyl alcohol, dehydrated alcohol, ferrosoferric oxide, isopropyl alcohol, potassium hydroxide, propylene glycol, purified water, shellac, and strong ammonia solution.</Description>
</NDC>
<NDC>
<NDCCode>51662-1325-1</NDCCode>
<PackageDescription>1 mL in 1 VIAL, SINGLE-DOSE (51662-1325-1) </PackageDescription>
<NDC11Code>51662-1325-01</NDC11Code>
<ProductNDC>51662-1325</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Ephedrine Sulfate</ProprietaryName>
<NonProprietaryName>Ephedrine Sulfate</NonProprietaryName>
<DosageFormName>INJECTION, SOLUTION</DosageFormName>
<RouteName>INTRAVENOUS</RouteName>
<StartMarketingDate>20181021</StartMarketingDate>
<MarketingCategoryName>NDA</MarketingCategoryName>
<ApplicationNumber>NDA208943</ApplicationNumber>
<LabelerName>HF Acquisition Co LLC, DBA HealthFirst</LabelerName>
<SubstanceName>EPHEDRINE SULFATE</SubstanceName>
<StrengthNumber>50</StrengthNumber>
<StrengthUnit>mg/mL</StrengthUnit>
<Pharm_Classes>Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Increased Norepinephrine Activity [PE], Norepinephrine Releasing Agent [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]</Pharm_Classes>
<Status>Active</Status>
<LastUpdate>2024-02-28</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20181021</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>Ephedrine sulfate injection is indicated for the treatment of clinically important hypotension occurring in the setting of anesthesia.</IndicationAndUsage>
<Description>Ephedrine sulfate is an alpha- and beta-adrenergic agonist and a norepinephrine-releasing agent. Ephedrine sulfate injection, USP is a clear, colorless, sterile solution for intravenous injection. Each mL contains ephedrine sulfate 50 mg in water for injection as a single-dose product. The pH range is 4.5 to 7.0. The drug product must be diluted before intravenous administration. The chemical name of ephedrine sulfate is (1R,2S)-(-)-2-methylamine-1-phenylpropan-1-ol sulfate (2:1) (salt). Its molecular weight is 428.54. The structural formula is. Image 1. Ephedrine sulfate darkens on exposure to light. It is freely soluble in water and ethanol, very slightly soluble in chloroform, and practically insoluble in ether.</Description>
</NDC>
<NDC>
<NDCCode>43742-0001-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0001-1)</PackageDescription>
<NDC11Code>43742-0001-01</NDC11Code>
<ProductNDC>43742-0001</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Rheumatism</ProprietaryName>
<NonProprietaryName>Benzoicum Acidum, Pulsatilla, Rhododendron Chrysanthum, Spiraea Ulmaria, Aconitum Napellus, Dulcamara, Euphorbium Officinarum, Ledum Palustre, Asclepias Tuberosa, Lithium Benzoicum,</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120405</StartMarketingDate>
<EndMarketingDate>20200925</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>BENZOIC ACID; PULSATILLA VULGARIS; RHODODENDRON AUREUM LEAF; FILIPENDULA ULMARIA ROOT; ACONITUM NAPELLUS; SOLANUM DULCAMARA FLOWER; EUPHORBIA RESINIFERA RESIN; LEDUM PALUSTRE TWIG; ASCLEPIAS TUBEROSA ROOT; LITHIUM BENZOATE</SubstanceName>
<StrengthNumber>3; 3; 3; 3; 4; 4; 4; 4; 6; 8</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2020-09-26</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0005-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0005-1)</PackageDescription>
<NDC11Code>43742-0005-01</NDC11Code>
<ProductNDC>43742-0005</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>B Complex Mix</ProprietaryName>
<NonProprietaryName>Magnesium Oroticum, Beta Vulgaris, Ascorbicum Acidum, Citricum Acidum, Cysteinum, Pulsatilla, Adenine, Amygdalin, Atp, Cholinum, Cyanocopalamin, Folic Acid, Insotil, Niacin, P-aminobenzoic Acid, Pangamic Acid, Panthothenic Acid,</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120416</StartMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>MAGNESIUM OROTATE; BETA VULGARIS; ASCORBIC ACID; ANHYDROUS CITRIC ACID; CYSTEINE; PULSATILLA VULGARIS; ADENINE; AMYGDALIN; ADENOSINE TRIPHOSPHATE; CHOLINE HYDROXIDE; CYANOCOBALAMIN; FOLIC ACID; INOSITOL; NIACIN; AMINOBENZOIC ACID; PANGAMIC ACID; PANTOTHENIC ACID; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SULFUR; THIAMINE; SODIUM DIETHYL OXALACETATE; OROTIC ACID MONOHYDRATE; MANGANESE PHOSPHATE, DIBASIC; ESCHERICHIA COLI; PROTEUS MORGANII</SubstanceName>
<StrengthNumber>12; 2; 3; 4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 7; 8; 10; 30; 30</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2018-10-30</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>43742-0006-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0006-1)</PackageDescription>
<NDC11Code>43742-0006-01</NDC11Code>
<ProductNDC>43742-0006</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Insect Bite</ProprietaryName>
<NonProprietaryName>Hypericum Perforatum, Ledum Palustre, Latrodectus Mactans, Loxosceles Reclusa, Tarentula Cubensis, Tarentula Hispana, Lachesis Mutus, Lycopus Virginicus, Theridion, Cimex Lectularius, Formica Rufa, Pulex Irritans, Vespa Crabro</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20110926</StartMarketingDate>
<EndMarketingDate>20200915</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc</LabelerName>
<SubstanceName>HYPERICUM PERFORATUM; LEDUM PALUSTRE TWIG; LATRODECTUS MACTANS; CITHARACANTHUS SPINICRUS; LYCOSA TARANTULA; LACHESIS MUTA VENOM; LYCOPUS VIRGINICUS; THERIDION CURASSAVICUM; CIMEX LECTULARIUS; FORMICA RUFA; PULEX IRRITANS; VESPA CRABRO; LOXOSCELES RECLUSA</SubstanceName>
<StrengthNumber>3; 4; 8; 8; 8; 10; 12; 12; 15; 15; 15; 15; 12</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2020-09-16</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0008-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0008-1)</PackageDescription>
<NDC11Code>43742-0008-01</NDC11Code>
<ProductNDC>43742-0008</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Heart Fatigue</ProprietaryName>
<NonProprietaryName>Spigelia Anthelmia, Kali Carbonicum, Arnica Montana, Cactus Grandiflorus, Gelsemium Sempervirens, Castoreum, Glonoinum, Ranunculus Bulbosus, Heart (suis), Abrotanum, Sulphur</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120418</StartMarketingDate>
<EndMarketingDate>20210422</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>SPIGELIA ANTHELMIA; POTASSIUM CARBONATE; ARNICA MONTANA; SELENICEREUS GRANDIFLORUS STEM; GELSEMIUM SEMPERVIRENS ROOT; CASTOR CANADENSIS SCENT GLAND SECRETION; NITROGLYCERIN; RANUNCULUS BULBOSUS; PORK HEART; ARTEMISIA ABROTANUM FLOWERING TOP; SULFUR</SubstanceName>
<StrengthNumber>2; 3; 4; 4; 4; 6; 6; 6; 8; 12; 12</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2021-04-23</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0011-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0011-1)</PackageDescription>
<NDC11Code>43742-0011-01</NDC11Code>
<ProductNDC>43742-0011</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Lymph Spleen Combo</ProprietaryName>
<NonProprietaryName>Castanea Vesca, Juniperus Communis, Phytolacca Decandra, Quercus Glandium Spiritus, Myosotis Arvensis, Natrum Sulphuricum, Ceanothus Americanus, Helianthus Annuus, Natrum Muriaticum, Lymph (suis), Spleen (suis), Thymus (suis),</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120501</StartMarketingDate>
<EndMarketingDate>20180806</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>CASTANEA SATIVA LEAF; JUNIPER BERRY; PHYTOLACCA AMERICANA ROOT; QUERCUS ROBUR NUT; MYOSOTIS ARVENSIS; SODIUM SULFATE; CEANOTHUS AMERICANUS LEAF; HELIANTHUS ANNUUS FLOWERING TOP; SODIUM CHLORIDE; SUS SCROFA LYMPH; SUS SCROFA SPLEEN; SUS SCROFA THYMUS; QUININE ARSENATE; ADENOSINE TRIPHOSPHATE; UBIDECARENONE; IRON; AMBER; APIS MELLIFERA</SubstanceName>
<StrengthNumber>3; 3; 3; 4; 6; 6; 6; 6; 6; 8; 8; 8; 8; 12; 12; 30; 30; 200</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2018-08-06</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0013-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0013-1)</PackageDescription>
<NDC11Code>43742-0013-01</NDC11Code>
<ProductNDC>43742-0013</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Celeragesic</ProprietaryName>
<NonProprietaryName>Cchinacea, Echinacea Purpurea, Hamamelis Virginiana, Bellis Perennis, Calendula Officinalis, Aconitum Napellus, Chamomilla, Hypericum Perforatum, Belladonna, Millefolium, Bryonia, Rhus Toxicodendron, Atp, Coenzyme A,</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120430</StartMarketingDate>
<EndMarketingDate>20180702</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>ECHINACEA, UNSPECIFIED; ECHINACEA PURPUREA; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; BELLIS PERENNIS; CALENDULA OFFICINALIS FLOWERING TOP; ACONITUM NAPELLUS; MATRICARIA RECUTITA; HYPERICUM PERFORATUM; ATROPA BELLADONNA; ACHILLEA MILLEFOLIUM; BRYONIA ALBA ROOT; ARNICA MONTANA; TOXICODENDRON PUBESCENS LEAF; ADENOSINE TRIPHOSPHATE; COENZYME A; CALCIUM SULFIDE; MERCURIUS SOLUBILIS; NADIDE; ORNITHOGALUM UMBELLATUM; HELIANTHEMUM NUMMULARIUM FLOWER; IMPATIENS GLANDULIFERA FLOWER; PRUNUS CERASIFERA FLOWER; CLEMATIS VITALBA FLOWER; LACTIC ACID, L-; COMFREY ROOT; ACTIVATED CHARCOAL; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; SUS SCROFA THALAMUS; PROTEUS MORGANII; UBIDECARENONE</SubstanceName>
<StrengthNumber>2; 2; 2; 2; 2; 3; 3; 3; 3; 3; 4; 4; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 12; 12; 12; 12; 30; 8</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2018-07-02</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0030-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0030-1)</PackageDescription>
<NDC11Code>43742-0030-01</NDC11Code>
<ProductNDC>43742-0030</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Matrix Support</ProprietaryName>
<NonProprietaryName>Ceanothus Americanus, Hydrastis Canadensis, Veratrum Album, Anacardium Orientale, Argentum Nitricum, Condurango, Momordica Balsamina, Oxalis Acetosella, Pulsatilla, Bile Duct (suis), Colon (suis), Duodenum (suis), Esophagus (suis), Eye (suis), Gallbladder (suis), Ileum (suis), Intestine (suis), Ipecacuanha, Jejunum (suis), Kali Bichromicum, Lung (suis), Mucosa Nasalis Suis, Natrum Oxalaceticum, Oral Mucosa (suis), Pancreas Suis, Phosphorus, Rectum (suis), Stomach (suis), Sulphur, Mannan</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120514</StartMarketingDate>
<EndMarketingDate>20200915</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>CEANOTHUS AMERICANUS LEAF; GOLDENSEAL; VERATRUM ALBUM ROOT; SEMECARPUS ANACARDIUM JUICE; SILVER NITRATE; MARSDENIA CONDURANGO BARK; MOMORDICA BALSAMINA IMMATURE FRUIT; OXALIS ACETOSELLA LEAF; PULSATILLA VULGARIS; SUS SCROFA BILE DUCT; SUS SCROFA COLON; SUS SCROFA DUODENUM; SUS SCROFA ESOPHAGUS; SUS SCROFA EYE; SUS SCROFA GALLBLADDER; SUS SCROFA ILEUM; PORK INTESTINE; IPECAC; SUS SCROFA JEJUNUM; POTASSIUM DICHROMATE; SUS SCROFA LUNG; SUS SCROFA NASAL MUCOSA; SODIUM DIETHYL OXALACETATE; SUS SCROFA ORAL MUCOSA; SUS SCROFA PANCREAS; PHOSPHORUS; SUS SCROFA RECTUM; SUS SCROFA STOMACH; SULFUR; YEAST MANNAN; ATROPA BELLADONNA; WOOD CREOSOTE; LACHESIS MUTA VENOM; MANDRAGORA OFFICINARUM ROOT; SUS SCROFA URINARY BLADDER; SHIGELLA DYSENTERIAE</SubstanceName>
<StrengthNumber>4; 4; 4; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 10; 10; 10; 10; 6; 30</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2020-09-16</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0050-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0050-1)</PackageDescription>
<NDC11Code>43742-0050-01</NDC11Code>
<ProductNDC>43742-0050</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Circulation</ProprietaryName>
<NonProprietaryName>Cactus Grandiflorus, Kali Carbonicum, Kalmia Latifolia, Arnica Montana, Glonoinum, Ignatia Amara, Lacticum Acidum, Ranunculus Bulbosus, Alpha-ketoglutaricum Acidum, Arsenicum Album, Cor (suis), Fumaricum Acidum, Hepar Suis, Malic Acid, Natrum Oxalaceticum, Phosphorus, Strophanthus Hispidus, Spigelia Anthelmia, Carbo Vegetabilis, Naja Tripudians, Cytomegalovirus, Epstein-barr Virus</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120601</StartMarketingDate>
<EndMarketingDate>20200918</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals</LabelerName>
<SubstanceName>SELENICEREUS GRANDIFLORUS STEM; POTASSIUM CARBONATE; KALMIA LATIFOLIA LEAF; ARNICA MONTANA; NITROGLYCERIN; STRYCHNOS IGNATII SEED; LACTIC ACID, DL-; RANUNCULUS BULBOSUS; .ALPHA.-KETOGLUTARIC ACID; ARSENIC TRIOXIDE; PORK HEART; FUMARIC ACID; PORK LIVER; MALIC ACID; SODIUM DIETHYL OXALACETATE; PHOSPHORUS; STROPHANTHUS HISPIDUS SEED; SPIGELIA ANTHELMIA; ACTIVATED CHARCOAL; NAJA NAJA VENOM; HUMAN HERPESVIRUS 5; HUMAN HERPESVIRUS 4</SubstanceName>
<StrengthNumber>3; 4; 4; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 10; 12; 15; 17; 17</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2020-09-19</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0053-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0053-1)</PackageDescription>
<NDC11Code>43742-0053-01</NDC11Code>
<ProductNDC>43742-0053</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Spine And Nerve Balance Core Formula</ProprietaryName>
<NonProprietaryName>Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Cuprum Aceticum, Nadidum, Natrum Oxalaceticum, Nicotinamidum, Picricum Acidum Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (suis), Silicea, Argentum Metallicum, Calcarea Phosphorica, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20140306</StartMarketingDate>
<EndMarketingDate>20200930</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals Inc.</LabelerName>
<SubstanceName>BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; LEDUM PALUSTRE TWIG; RANUNCULUS BULBOSUS; HORSE CHESTNUT; CUPRIC ACETATE; NADIDE; SODIUM DIETHYL OXALACETATE; NIACINAMIDE; PICRIC ACID; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE; .ALPHA.-LIPOIC ACID; AMMONIUM CHLORIDE; SUS SCROFA CARTILAGE; SUS SCROFA INTERVERTEBRAL DISC; SILICON DIOXIDE; SILVER; TRIBASIC CALCIUM PHOSPHATE; COENZYME A; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; PSEUDOGNAPHALIUM OBTUSIFOLIUM; SUS SCROFA BONE MARROW; MERCURIC OXIDE; SULFUR; ENTEROBACTER CLOACAE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; PROTEUS MORGANII; PROTEUS VULGARIS</SubstanceName>
<StrengthNumber>4; 4; 4; 4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 10; 10; 10; 10; 10; 10; 10; 10; 28; 30; 30; 30; 30</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2020-10-01</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0056-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0056-1)</PackageDescription>
<NDC11Code>43742-0056-01</NDC11Code>
<ProductNDC>43742-0056</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Post-dental Visit</ProprietaryName>
<NonProprietaryName>Chamomilla, Echinacea, Hamamelis Virginiana, Hypericum Perforatum, Millefolium, Bryonia, Calendula Officinalis, Arnica Montana, Belladonna, Bellis Perennis, Rhus Toxicodendron, Hepar Sulphuris Calcareum, Star Of Bethleham, Rock Rose, Impatiens, Cherry Plum, Clematis, Carbo Vegetabilis</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120618</StartMarketingDate>
<EndMarketingDate>20190114</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>MATRICARIA RECUTITA; ECHINACEA, UNSPECIFIED; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; HYPERICUM PERFORATUM; ACHILLEA MILLEFOLIUM; BRYONIA ALBA ROOT; CALENDULA OFFICINALIS FLOWERING TOP; ARNICA MONTANA; ATROPA BELLADONNA; BELLIS PERENNIS; TOXICODENDRON PUBESCENS LEAF; CALCIUM SULFIDE; ORNITHOGALUM UMBELLATUM; HELIANTHEMUM NUMMULARIUM FLOWER; IMPATIENS GLANDULIFERA FLOWER; PRUNUS CERASIFERA FLOWER; CLEMATIS VITALBA FLOWER; ACTIVATED CHARCOAL</SubstanceName>
<StrengthNumber>3; 3; 3; 3; 3; 4; 4; 4; 6; 6; 6; 8; 8; 8; 8; 8; 8; 12</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2019-01-14</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0060-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0060-1) </PackageDescription>
<NDC11Code>43742-0060-01</NDC11Code>
<ProductNDC>43742-0060</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Thyroplus</ProprietaryName>
<NonProprietaryName>Fucus Vesiculosus, Spongia Tosta, Phosphoricum Acidum, Pituitary (suis), Thyroidinum (suis), Calcarea Carbonica, Iodium, Iridium Metallicum</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120626</StartMarketingDate>
<EndMarketingDate>20201110</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>FUCUS VESICULOSUS; SPONGIA OFFICINALIS SKELETON, ROASTED; PHOSPHORIC ACID; SUS SCROFA PITUITARY GLAND; THYROID, PORCINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; IODINE; IRIDIUM</SubstanceName>
<StrengthNumber>3; 4; 6; 8; 8; 12; 12; 12</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2020-11-11</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20120626</StartMarketingDatePackage>
<EndMarketingDatePackage>20201110</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>43742-0061-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0061-1)</PackageDescription>
<NDC11Code>43742-0061-01</NDC11Code>
<ProductNDC>43742-0061</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Detox</ProprietaryName>
<ProprietaryNameSuffix>I</ProprietaryNameSuffix>
<NonProprietaryName>Carduus Marianus, Chelidonium Majus, Cinchona Officinalis, Lycopodium Clavatum, Taraxacum Officinale, Veratrum Album, Avena Sativa, Cynara Scolymus, Methylcobalamin, Menadione, Alpha-lipoicum Acidum, Hepar Suis, Colon (suis), Duodenum (suis), Gallbladder (suis), Intestine (suis), Lymph Node (suis), Pancreas Suis, Thymus (suis), Alpha-ketoglutaricum Acidum, Cholesterinum, Formicum Acidum, Glyoxal Trimer Dihydrate, Histaminum Hydrochloricum, Malic Acid, Natrum Oxalaceticum, Sulphur</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120629</StartMarketingDate>
<EndMarketingDate>20200925</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>SILYBUM MARIANUM SEED; CHELIDONIUM MAJUS; CINCHONA OFFICINALIS BARK; LYCOPODIUM CLAVATUM SPORE; TARAXACUM OFFICINALE; VERATRUM ALBUM ROOT; AVENA SATIVA FLOWERING TOP; CYNARA SCOLYMUS LEAF; METHYLCOBALAMIN; MENADIONE; .ALPHA.-LIPOIC ACID; PORK LIVER; SUS SCROFA COLON; SUS SCROFA DUODENUM; SUS SCROFA GALLBLADDER; PORK INTESTINE; SUS SCROFA LYMPH; SUS SCROFA PANCREAS; SUS SCROFA THYMUS; .ALPHA.-KETOGLUTARIC ACID; CHOLESTEROL; FORMIC ACID; GLYOXAL TRIMER DIHYDRATE; HISTAMINE DIHYDROCHLORIDE; MALIC ACID; SODIUM DIETHYL OXALACETATE; SULFUR; OYSTER SHELL CALCIUM CARBONATE, CRUDE; OROTIC ACID MONOHYDRATE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; PROTEUS MORGANII</SubstanceName>
<StrengthNumber>3; 4; 4; 4; 4; 4; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 10; 10; 10; 10; 10; 10; 10; 13; 28; 7; 30; 30</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2020-09-26</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0062-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0062-1)</PackageDescription>
<NDC11Code>43742-0062-01</NDC11Code>
<ProductNDC>43742-0062</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Detox</ProprietaryName>
<ProprietaryNameSuffix>Iii</ProprietaryNameSuffix>
<NonProprietaryName>Conium Maculatum, Dulcamara, Echinacea, Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbicum Acidum, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Lymph (suis), Sulphur, Glandula Suprarenalis Suis, Phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus (suis), Spleen (suis) Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Funiculus Umbilicalis Suis, Tonsil (suis), Gaertner Bach, Triiodothyronine, Medulla Ossis Suis, Mutabile Bach</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120628</StartMarketingDate>
<EndMarketingDate>20171003</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>CONIUM MACULATUM FLOWERING TOP; SOLANUM DULCAMARA TOP; ECHINACEA, UNSPECIFIED; HORSE CHESTNUT; ANTIMONY POTASSIUM TARTRATE; ASCORBIC ACID; PROTORTONIA CACTI; GALIUM APARINE; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; PULSATILLA VULGARIS; LACTIC ACID, L-; SUS SCROFA LYMPH; SULFUR; SUS SCROFA ADRENAL GLAND; PHENYLALANINE; TRIBASIC CALCIUM PHOSPHATE; FERROSOFERRIC PHOSPHATE; PORK LIVER; SUS SCROFA HYPOTHALAMUS; SUS SCROFA SPLEEN; CORTISONE ACETATE; MERCURIUS SOLUBILIS; BARIUM CARBONATE; SUS SCROFA UMBILICAL CORD; SUS SCROFA TONSIL; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; LIOTHYRONINE; SUS SCROFA BONE MARROW; ESCHERICHIA COLI</SubstanceName>
<StrengthNumber>4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 10; 10; 10; 10; 10; 13; 13; 28; 6; 6; 9; 10; 12; 30</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2017-10-05</LastUpdate>
</NDC>
<NDC>
<NDCCode>43742-0072-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0072-1)</PackageDescription>
<NDC11Code>43742-0072-01</NDC11Code>
<ProductNDC>43742-0072</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Spinalmax</ProprietaryName>
<NonProprietaryName>Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Cuprum Aceticum, Nadidum, Natrum Oxalaceticum, Nicotinamidum, Picricum Acidum, Pyridoxinum, Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (suis), Silicea, Argentum Metallicum, Calcarea Phosphorica, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20140402</StartMarketingDate>
<EndMarketingDate>20200913</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; LEDUM PALUSTRE TWIG; RANUNCULUS BULBOSUS; HORSE CHESTNUT; CUPRIC ACETATE; NADIDE; SODIUM DIETHYL OXALACETATE; NIACINAMIDE; PICRIC ACID; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE HYDROCHLORIDE; .ALPHA.-LIPOIC ACID; AMMONIUM CHLORIDE; SUS SCROFA CARTILAGE; SUS SCROFA INTERVERTEBRAL DISC; SILICON DIOXIDE; SILVER; TRIBASIC CALCIUM PHOSPHATE; COENZYME A; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; PSEUDOGNAPHALIUM OBTUSIFOLIUM; SUS SCROFA BONE MARROW; MERCURIC OXIDE; SULFUR; ENTEROBACTER CLOACAE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; PROTEUS MORGANII; PROTEUS VULGARIS</SubstanceName>
<StrengthNumber>4; 4; 4; 4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 10; 10; 10; 10; 10; 10; 10; 10; 28; 30; 30; 30; 30</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2020-09-15</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0073-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0073-1) </PackageDescription>
<NDC11Code>43742-0073-01</NDC11Code>
<ProductNDC>43742-0073</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Detox</ProprietaryName>
<ProprietaryNameSuffix>Ii</ProprietaryNameSuffix>
<NonProprietaryName>Solidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, Equisetum Hyemale, Argentum Nitricum 6x, Cantharis, Capsicum Annuum, Cuprum Sulphuricum, Orthosiphon Stamineus, Pareira Brava, Sarsaparilla, Terebinthina, Apis Venenum Purum, Barosma, Mercurius Corrosivus, Pyelon (suis), Ureter (suis), Urethra (suis), Urinary Bladder (suis), Glyoxal Trimer Dihydrate, Hepar Sulphuris Calcareum, Natrum Pyruvicum, Quercetin, Colibacillinum Cum Natrum Muriaticum, Dysentery Bacillus</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120710</StartMarketingDate>
<EndMarketingDate>20200805</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>SOLIDAGO VIRGAUREA FLOWERING TOP; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; EQUISETUM HYEMALE; SILVER NITRATE; LYTTA VESICATORIA; CAPSICUM; CUPRIC SULFATE; CLERODENDRANTHUS SPICATUS LEAF; CHONDRODENDRON TOMENTOSUM ROOT; SMILAX ORNATA ROOT; TURPENTINE OIL; APIS MELLIFERA VENOM; AGATHOSMA BETULINA LEAF; MERCURIC CHLORIDE; SUS SCROFA RENAL PELVIS; SUS SCROFA URETER; SUS SCROFA URETHRA; SUS SCROFA URINARY BLADDER; GLYOXAL TRIMER DIHYDRATE; CALCIUM SULFIDE; SODIUM PYRUVATE; QUERCETIN; ESCHERICHIA COLI; SHIGELLA DYSENTERIAE</SubstanceName>
<StrengthNumber>3; 4; 4; 4; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 10; 10; 10; 10; 15; 30</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2020-08-06</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20120710</StartMarketingDatePackage>
<EndMarketingDatePackage>20200805</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>43742-0087-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0087-1)</PackageDescription>
<NDC11Code>43742-0087-01</NDC11Code>
<ProductNDC>43742-0087</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Intestinal Distress</ProprietaryName>
<NonProprietaryName>Echinacea, Colchicum Autumnale, Aloe Socotrina, Colocynthis, Mercurius Corrosivus, Nux Vomica, Arsenicum Album</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120821</StartMarketingDate>
<EndMarketingDate>20171015</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>ECHINACEA ANGUSTIFOLIA; COLCHICUM AUTUMNALE BULB; ALOE; CITRULLUS COLOCYNTHIS FRUIT PULP; MERCURIC CHLORIDE; STRYCHNOS NUX-VOMICA SEED; ARSENIC TRIOXIDE; QUININE SULFATE; VIBRIO CHOLERAE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; CAMPYLOBACTER JEJUNI; ESCHERICHIA COLI; HELICOBACTER PYLORI; SHIGELLA DYSENTERIAE; YERSINIA ENTEROCOLITICA; BOTULINUM TOXIN TYPE A; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR TYPHI</SubstanceName>
<StrengthNumber>3; 4; 6; 6; 6; 6; 6; 12; 12; 15; 30; 30; 30; 30; 30; 30; 33</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2017-10-19</LastUpdate>
</NDC>
<NDC>
<NDCCode>43742-0090-1</NDCCode>
<PackageDescription>60 mL in 1 BOTTLE, DROPPER (43742-0090-1)</PackageDescription>
<NDC11Code>43742-0090-01</NDC11Code>
<ProductNDC>43742-0090</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Lymph Drainage</ProprietaryName>
<NonProprietaryName>Citrus Limonum, Echinacea, Scrophularia Nodosa, Teucrium Scorodonia, Baptisia Tinctoria, Lobelia Inflata, Phytolacca Decandra</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120821</StartMarketingDate>
<EndMarketingDate>20171108</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>LEMON JUICE; ECHINACEA, UNSPECIFIED; SCROPHULARIA NODOSA; TEUCRIUM SCORODONIA FLOWERING TOP; BAPTISIA TINCTORIA; LOBELIA INFLATA; PHYTOLACCA AMERICANA ROOT; PINUS SYLVESTRIS LEAFY TWIG; ZINC GLUCONATE; THUJA OCCIDENTALIS LEAFY TWIG; CAPSICUM; COPPER GLUCONATE; MAGNESIUM GLUCONATE; ARANEUS DIADEMATUS; ARSENIC TRIIODIDE; CENTAURIUM ERYTHRAEA; CARPINUS BETULUS FLOWER; LARIX DECIDUA FLOWERING TOP; SUS SCROFA LYMPH; SUS SCROFA SPLEEN; SUS SCROFA THYMUS; LACHESIS MUTA VENOM</SubstanceName>
<StrengthNumber>1; 1; 1; 1; 1; 3; 3; 3; 3; 4; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 12</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2017-11-08</LastUpdate>
</NDC>
<NDC>
<NDCCode>43742-0111-1</NDCCode>
<PackageDescription>960 mL in 1 PACKAGE (43742-0111-1)</PackageDescription>
<NDC11Code>43742-0111-01</NDC11Code>
<ProductNDC>43742-0111</ProductNDC>
<ProductTypeName>BULK INGREDIENT</ProductTypeName>
<NonProprietaryName>Astragalus Membranaceus, Baptisia Tinctoria, Condurango, Echinacea (angustifolia), Hydrastis Canadensis, Nasturtium Aquaticum, Osha, Phytolacca Decandra, Propolis, Thymus (suis), Aranea Diadema, Gelsemium Sempervirens, Iodium, Ipecacuanha, Lycopodium Clavatum, Mercurius Solubilis, Muriaticum Acidum, Nitricum Acidum, Rhus Tox, Silicea Tabebuia Impetiginosa, Epstein-barr Virus Nosode</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<StartMarketingDate>20140904</StartMarketingDate>
<EndMarketingDate>20191114</EndMarketingDate>
<MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
<LabelerName>Deseret Biologicals</LabelerName>
<SubstanceName>ASTRAGALUS PROPINQUUS ROOT; BAPTISIA TINCTORIA ROOT; MARSDENIA CONDURANGO BARK; ECHINACEA, UNSPECIFIED; GOLDENSEAL; NASTURTIUM OFFICINALE; LIGUSTICUM PORTERI ROOT; PHYTOLACCA AMERICANA ROOT; PROPOLIS WAX; SUS SCROFA THYMUS; ARANEUS DIADEMATUS; GELSEMIUM SEMPERVIRENS ROOT; IODINE; IPECAC; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; HYDROCHLORIC ACID; NITRIC ACID; TOXICODENDRON PUBESCENS LEAF; SILICON DIOXIDE; TABEBUIA IMPETIGINOSA BARK; HUMAN HERPESVIRUS 4</SubstanceName>
<StrengthNumber>6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 30</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2014-02-04</LastUpdate>
<ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>43742-0126-1</NDCCode>
<PackageDescription>960 mL in 1 BOTTLE (43742-0126-1)</PackageDescription>
<NDC11Code>43742-0126-01</NDC11Code>
<ProductNDC>43742-0126</ProductNDC>
<ProductTypeName>DRUG FOR FURTHER PROCESSING</ProductTypeName>
<NonProprietaryName>Echinacea (angustifolia), Hydrastis Canadensis, Nasturtium Aquaticum, Thuja Occidentalis, Thymus (suis), Belladonna, Eupatorium Perfoliatum, Gelsemium Sempervirens, Iodium, Lachesis Mutus, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Selenium Metallicum, Zincum Metallicum, Cytomegalovirus Nosode, Herpes Simplex 1 Nosode, Herpes Simplex 2 Nosode, Herpes Zoster Nosode, Poliomyelitis Nosode, Epstein Barr Virus Nosode, Morbillinum, Parotidinum, Rubella Nosode, Pyrogenium</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<StartMarketingDate>20120829</StartMarketingDate>
<EndMarketingDate>20220427</EndMarketingDate>
<MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>ECHINACEA ANGUSTIFOLIA; GOLDENSEAL; NASTURTIUM OFFICINALE; THUJA OCCIDENTALIS LEAFY TWIG; SUS SCROFA THYMUS; ATROPA BELLADONNA; EUPATORIUM PERFOLIATUM FLOWERING TOP; GELSEMIUM SEMPERVIRENS ROOT; IODINE; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; PHOSPHORIC ACID; PHOSPHORUS; SELENIUM; ZINC; HUMAN HERPESVIRUS 5; HUMAN HERPESVIRUS 1; HUMAN HERPESVIRUS 2; HUMAN HERPESVIRUS 3; POLIOVIRUS; HUMAN HERPESVIRUS 4; MEASLES VIRUS; MUMPS VIRUS; RUBELLA VIRUS; RANCID BEEF; HEPATITIS B VIRUS; HUMAN COXSACKIEVIRUS B1; HUMAN COXSACKIEVIRUS B4; ANTIMONY TRISULFIDE; LEDUM PALUSTRE TWIG; THIMEROSAL</SubstanceName>
<StrengthNumber>6; 6; 6; 6; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 15; 15; 15; 15; 18; 30; 30; 30; 30; 33; 8; 8; 30; 30; 30</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2014-02-04</LastUpdate>
</NDC>
<NDC>
<NDCCode>43742-0130-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0130-1)</PackageDescription>
<NDC11Code>43742-0130-01</NDC11Code>
<ProductNDC>43742-0130</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Sinusitis</ProprietaryName>
<NonProprietaryName>Pulsatilla, Plantago Major, Euphorbium Officinarum, Luffa Operculata, Mercurius Iodatus Ruber, Mucosa Nasalis Suis, Argentum Nitricum</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120906</StartMarketingDate>
<EndMarketingDate>20180905</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>PULSATILLA VULGARIS; PLANTAGO MAJOR; EUPHORBIA RESINIFERA RESIN; LUFFA OPERCULATA FRUIT; MERCURIC IODIDE; SUS SCROFA NASAL MUCOSA; SILVER NITRATE; CALCIUM SULFIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SODIUM CHLORIDE; SINUSITISINUM</SubstanceName>
<StrengthNumber>2; 3; 4; 6; 8; 8; 10; 10; 12; 12; 18</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2018-09-07</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>43742-0131-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0131-1) </PackageDescription>
<NDC11Code>43742-0131-01</NDC11Code>
<ProductNDC>43742-0131</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Tobacco</ProprietaryName>
<NonProprietaryName>Avena Sativa, Lobelia Inflata, Cactus Grandiflorus, Tabacum, Gelsemium Sempervirens, Selenium Metallicum, Staphysagria, Vanadium Metallicum</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120920</StartMarketingDate>
<EndMarketingDate>20220713</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>AVENA SATIVA FLOWERING TOP; DELPHINIUM STAPHISAGRIA SEED; GELSEMIUM SEMPERVIRENS ROOT; LOBELIA INFLATA; SELENICEREUS GRANDIFLORUS STEM; SELENIUM; TOBACCO LEAF; VANADIUM</SubstanceName>
<StrengthNumber>1; 12; 12; 3; 4; 12; 6; 12</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2022-07-14</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20170605</StartMarketingDatePackage>
<EndMarketingDatePackage>20220713</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>43742-0132-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (43742-0132-1)</PackageDescription>
<NDC11Code>43742-0132-01</NDC11Code>
<ProductNDC>43742-0132</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Ebv</ProprietaryName>
<NonProprietaryName>Baptisia Tinctoria, Condurango, Echinacea, Hydrastis Canadensis, Nasturtium Aquaticum, Osha, Phytolacca Decandra, Tabebuia Impetiginosa, Astragalus Menziesii, Propolis, Glandula Suprarenalis Suis, Thymus (suis), Aranea Diadema, Gelsemium Sempervirens, Ipecacuanha, Lycopodium Clavatum, Mercurius Solubilis, Muriaticum Acidum, Nitricum Acidum, Rhus Toxicodendron, Selenium Metallicum, Silicea, Epstein Barr Virus</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20120910</StartMarketingDate>
<EndMarketingDate>20180928</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Deseret Biologicals, Inc.</LabelerName>
<SubstanceName>BAPTISIA TINCTORIA; MARSDENIA CONDURANGO BARK; ECHINACEA, UNSPECIFIED; GOLDENSEAL; NASTURTIUM AQUATICUM; LIGUSTICUM PORTERI ROOT; PHYTOLACCA AMERICANA ROOT; TABEBUIA IMPETIGINOSA BARK; ASTRAGALUS NUTTALLII LEAF; PROPOLIS WAX; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYMUS; ARANEUS DIADEMATUS; GELSEMIUM SEMPERVIRENS ROOT; IPECAC; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; HYDROCHLORIC ACID; NITRIC ACID; TOXICODENDRON PUBESCENS LEAF; SELENIUM; SILICON DIOXIDE; HUMAN HERPESVIRUS 4</SubstanceName>
<StrengthNumber>3; 3; 3; 3; 3; 3; 3; 3; 6; 6; 8; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 30</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2018-09-29</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
</NDCList>
<NDCList><NDC><NDCCode>43742-1325-4</NDCCode><ProprietaryName>Rheumagesic</ProprietaryName><NonProprietaryName>Arnica Montana, Apis Mellifica, Benzoicum Acidum, Cartilago Suis, Ledum Palustre, Pantothenic Acid, Ruta Graveolens, Rhododendron Chrysanthum, Causticum, Formica Rufa, Sepia, Alpha-lipoicum Acidum, Aurum Metallicum, Calcarea Phosphorica, Colchicum Autumnale, Phytolacca Decandra, Radium Bromatum, Rhus Venenata, Thuja Occidentalis, Lac Caninum</NonProprietaryName></NDC><NDC><NDCCode>43742-0702-4</NDCCode><NonProprietaryName>Aconitum Napellus, Antimonium Tartaricum, Arsenicum Iodatum, Belladonna, Bryonia, Causticum, Coccus Cacti, Cuprum Aceticum, Drosera (rotundifolia), Hyoscyamus Niger, Ipecacuanha, Kreosotum, Lobelia Inflata, Phosphorus, Scilla Maritima, Sticta Pulmonaria, Silicea, Carbo Vegetabilis, Kali Carbonicum, Lachesis Mutus, Pertussinum, Tetanus Toxin</NonProprietaryName></NDC><NDC><NDCCode>22840-1325-4</NDCCode><ProprietaryName>Firebush Kochia</ProprietaryName><NonProprietaryName>Kochia Scoparia</NonProprietaryName></NDC><NDC><NDCCode>36987-1325-4</NDCCode><ProprietaryName>Fig</ProprietaryName><NonProprietaryName>Fig</NonProprietaryName></NDC><NDC><NDCCode>70771-1325-4</NDCCode><ProprietaryName>Candesartan Cilexetil And Hydrochlorothiazide</ProprietaryName><NonProprietaryName>Candesartan Cilexetil And Hydrochlorothiazide</NonProprietaryName></NDC><NDC><NDCCode>71335-1325-4</NDCCode><ProprietaryName>Hydroxyzine Pamoate</ProprietaryName><NonProprietaryName>Hydroxyzine Pamoate</NonProprietaryName></NDC><NDC><NDCCode>0115-1325-10</NDCCode><ProprietaryName>Fenofibric Acid</ProprietaryName><NonProprietaryName>Fenofibric Acid</NonProprietaryName></NDC><NDC><NDCCode>51662-1325-1</NDCCode><ProprietaryName>Ephedrine Sulfate</ProprietaryName><NonProprietaryName>Ephedrine Sulfate</NonProprietaryName></NDC><NDC><NDCCode>43742-0001-1</NDCCode><ProprietaryName>Rheumatism</ProprietaryName><NonProprietaryName>Benzoicum Acidum, Pulsatilla, Rhododendron Chrysanthum, Spiraea Ulmaria, Aconitum Napellus, Dulcamara, Euphorbium Officinarum, Ledum Palustre, Asclepias Tuberosa, Lithium Benzoicum,</NonProprietaryName></NDC><NDC><NDCCode>43742-0005-1</NDCCode><ProprietaryName>B Complex Mix</ProprietaryName><NonProprietaryName>Magnesium Oroticum, Beta Vulgaris, Ascorbicum Acidum, Citricum Acidum, Cysteinum, Pulsatilla, Adenine, Amygdalin, Atp, Cholinum, Cyanocopalamin, Folic Acid, Insotil, Niacin, P-aminobenzoic Acid, Pangamic Acid, Panthothenic Acid,</NonProprietaryName></NDC><NDC><NDCCode>43742-0006-1</NDCCode><ProprietaryName>Insect Bite</ProprietaryName><NonProprietaryName>Hypericum Perforatum, Ledum Palustre, Latrodectus Mactans, Loxosceles Reclusa, Tarentula Cubensis, Tarentula Hispana, Lachesis Mutus, Lycopus Virginicus, Theridion, Cimex Lectularius, Formica Rufa, Pulex Irritans, Vespa Crabro</NonProprietaryName></NDC><NDC><NDCCode>43742-0008-1</NDCCode><ProprietaryName>Heart Fatigue</ProprietaryName><NonProprietaryName>Spigelia Anthelmia, Kali Carbonicum, Arnica Montana, Cactus Grandiflorus, Gelsemium Sempervirens, Castoreum, Glonoinum, Ranunculus Bulbosus, Heart (suis), Abrotanum, Sulphur</NonProprietaryName></NDC><NDC><NDCCode>43742-0011-1</NDCCode><ProprietaryName>Lymph Spleen Combo</ProprietaryName><NonProprietaryName>Castanea Vesca, Juniperus Communis, Phytolacca Decandra, Quercus Glandium Spiritus, Myosotis Arvensis, Natrum Sulphuricum, Ceanothus Americanus, Helianthus Annuus, Natrum Muriaticum, Lymph (suis), Spleen (suis), Thymus (suis),</NonProprietaryName></NDC><NDC><NDCCode>43742-0013-1</NDCCode><ProprietaryName>Celeragesic</ProprietaryName><NonProprietaryName>Cchinacea, Echinacea Purpurea, Hamamelis Virginiana, Bellis Perennis, Calendula Officinalis, Aconitum Napellus, Chamomilla, Hypericum Perforatum, Belladonna, Millefolium, Bryonia, Rhus Toxicodendron, Atp, Coenzyme A,</NonProprietaryName></NDC><NDC><NDCCode>43742-0030-1</NDCCode><ProprietaryName>Matrix Support</ProprietaryName><NonProprietaryName>Ceanothus Americanus, Hydrastis Canadensis, Veratrum Album, Anacardium Orientale, Argentum Nitricum, Condurango, Momordica Balsamina, Oxalis Acetosella, Pulsatilla, Bile Duct (suis), Colon (suis), Duodenum (suis), Esophagus (suis), Eye (suis), Gallbladder (suis), Ileum (suis), Intestine (suis), Ipecacuanha, Jejunum (suis), Kali Bichromicum, Lung (suis), Mucosa Nasalis Suis, Natrum Oxalaceticum, Oral Mucosa (suis), Pancreas Suis, Phosphorus, Rectum (suis), Stomach (suis), Sulphur, Mannan</NonProprietaryName></NDC><NDC><NDCCode>43742-0050-1</NDCCode><ProprietaryName>Circulation</ProprietaryName><NonProprietaryName>Cactus Grandiflorus, Kali Carbonicum, Kalmia Latifolia, Arnica Montana, Glonoinum, Ignatia Amara, Lacticum Acidum, Ranunculus Bulbosus, Alpha-ketoglutaricum Acidum, Arsenicum Album, Cor (suis), Fumaricum Acidum, Hepar Suis, Malic Acid, Natrum Oxalaceticum, Phosphorus, Strophanthus Hispidus, Spigelia Anthelmia, Carbo Vegetabilis, Naja Tripudians, Cytomegalovirus, Epstein-barr Virus</NonProprietaryName></NDC><NDC><NDCCode>43742-0053-1</NDCCode><ProprietaryName>Spine And Nerve Balance Core Formula</ProprietaryName><NonProprietaryName>Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Cuprum Aceticum, Nadidum, Natrum Oxalaceticum, Nicotinamidum, Picricum Acidum Pyridoxinum Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (suis), Silicea, Argentum Metallicum, Calcarea Phosphorica, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis</NonProprietaryName></NDC><NDC><NDCCode>43742-0056-1</NDCCode><ProprietaryName>Post-dental Visit</ProprietaryName><NonProprietaryName>Chamomilla, Echinacea, Hamamelis Virginiana, Hypericum Perforatum, Millefolium, Bryonia, Calendula Officinalis, Arnica Montana, Belladonna, Bellis Perennis, Rhus Toxicodendron, Hepar Sulphuris Calcareum, Star Of Bethleham, Rock Rose, Impatiens, Cherry Plum, Clematis, Carbo Vegetabilis</NonProprietaryName></NDC><NDC><NDCCode>43742-0060-1</NDCCode><ProprietaryName>Thyroplus</ProprietaryName><NonProprietaryName>Fucus Vesiculosus, Spongia Tosta, Phosphoricum Acidum, Pituitary (suis), Thyroidinum (suis), Calcarea Carbonica, Iodium, Iridium Metallicum</NonProprietaryName></NDC><NDC><NDCCode>43742-0061-1</NDCCode><ProprietaryName>Detox</ProprietaryName><NonProprietaryName>Carduus Marianus, Chelidonium Majus, Cinchona Officinalis, Lycopodium Clavatum, Taraxacum Officinale, Veratrum Album, Avena Sativa, Cynara Scolymus, Methylcobalamin, Menadione, Alpha-lipoicum Acidum, Hepar Suis, Colon (suis), Duodenum (suis), Gallbladder (suis), Intestine (suis), Lymph Node (suis), Pancreas Suis, Thymus (suis), Alpha-ketoglutaricum Acidum, Cholesterinum, Formicum Acidum, Glyoxal Trimer Dihydrate, Histaminum Hydrochloricum, Malic Acid, Natrum Oxalaceticum, Sulphur</NonProprietaryName></NDC><NDC><NDCCode>43742-0062-1</NDCCode><ProprietaryName>Detox</ProprietaryName><NonProprietaryName>Conium Maculatum, Dulcamara, Echinacea, Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbicum Acidum, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Lymph (suis), Sulphur, Glandula Suprarenalis Suis, Phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus (suis), Spleen (suis) Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Funiculus Umbilicalis Suis, Tonsil (suis), Gaertner Bach, Triiodothyronine, Medulla Ossis Suis, Mutabile Bach</NonProprietaryName></NDC><NDC><NDCCode>43742-0072-1</NDCCode><ProprietaryName>Spinalmax</ProprietaryName><NonProprietaryName>Berberis Vulgaris, Cimicifuga Racemosa, Cinchona Officinalis, Colocynthis, Ledum Palustre, Ranunculus Bulbosus, Aesculus Hippocastanum, Cuprum Aceticum, Nadidum, Natrum Oxalaceticum, Nicotinamidum, Picricum Acidum, Pyridoxinum, Hydrochloricum, Riboflavinum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Ammonium Muriaticum, Cartilago Suis, Discus Intervertebralis (suis), Silicea, Argentum Metallicum, Calcarea Phosphorica, Coenzyme A, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis</NonProprietaryName></NDC><NDC><NDCCode>43742-0073-1</NDCCode><ProprietaryName>Detox</ProprietaryName><NonProprietaryName>Solidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, Equisetum Hyemale, Argentum Nitricum 6x, Cantharis, Capsicum Annuum, Cuprum Sulphuricum, Orthosiphon Stamineus, Pareira Brava, Sarsaparilla, Terebinthina, Apis Venenum Purum, Barosma, Mercurius Corrosivus, Pyelon (suis), Ureter (suis), Urethra (suis), Urinary Bladder (suis), Glyoxal Trimer Dihydrate, Hepar Sulphuris Calcareum, Natrum Pyruvicum, Quercetin, Colibacillinum Cum Natrum Muriaticum, Dysentery Bacillus</NonProprietaryName></NDC><NDC><NDCCode>43742-0087-1</NDCCode><ProprietaryName>Intestinal Distress</ProprietaryName><NonProprietaryName>Echinacea, Colchicum Autumnale, Aloe Socotrina, Colocynthis, Mercurius Corrosivus, Nux Vomica, Arsenicum Album</NonProprietaryName></NDC><NDC><NDCCode>43742-0090-1</NDCCode><ProprietaryName>Lymph Drainage</ProprietaryName><NonProprietaryName>Citrus Limonum, Echinacea, Scrophularia Nodosa, Teucrium Scorodonia, Baptisia Tinctoria, Lobelia Inflata, Phytolacca Decandra</NonProprietaryName></NDC><NDC><NDCCode>43742-0111-1</NDCCode><NonProprietaryName>Astragalus Membranaceus, Baptisia Tinctoria, Condurango, Echinacea (angustifolia), Hydrastis Canadensis, Nasturtium Aquaticum, Osha, Phytolacca Decandra, Propolis, Thymus (suis), Aranea Diadema, Gelsemium Sempervirens, Iodium, Ipecacuanha, Lycopodium Clavatum, Mercurius Solubilis, Muriaticum Acidum, Nitricum Acidum, Rhus Tox, Silicea Tabebuia Impetiginosa, Epstein-barr Virus Nosode</NonProprietaryName></NDC><NDC><NDCCode>43742-0126-1</NDCCode><NonProprietaryName>Echinacea (angustifolia), Hydrastis Canadensis, Nasturtium Aquaticum, Thuja Occidentalis, Thymus (suis), Belladonna, Eupatorium Perfoliatum, Gelsemium Sempervirens, Iodium, Lachesis Mutus, Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Selenium Metallicum, Zincum Metallicum, Cytomegalovirus Nosode, Herpes Simplex 1 Nosode, Herpes Simplex 2 Nosode, Herpes Zoster Nosode, Poliomyelitis Nosode, Epstein Barr Virus Nosode, Morbillinum, Parotidinum, Rubella Nosode, Pyrogenium</NonProprietaryName></NDC><NDC><NDCCode>43742-0130-1</NDCCode><ProprietaryName>Sinusitis</ProprietaryName><NonProprietaryName>Pulsatilla, Plantago Major, Euphorbium Officinarum, Luffa Operculata, Mercurius Iodatus Ruber, Mucosa Nasalis Suis, Argentum Nitricum</NonProprietaryName></NDC><NDC><NDCCode>43742-0131-1</NDCCode><ProprietaryName>Tobacco</ProprietaryName><NonProprietaryName>Avena Sativa, Lobelia Inflata, Cactus Grandiflorus, Tabacum, Gelsemium Sempervirens, Selenium Metallicum, Staphysagria, Vanadium Metallicum</NonProprietaryName></NDC><NDC><NDCCode>43742-0132-1</NDCCode><ProprietaryName>Ebv</ProprietaryName><NonProprietaryName>Baptisia Tinctoria, Condurango, Echinacea, Hydrastis Canadensis, Nasturtium Aquaticum, Osha, Phytolacca Decandra, Tabebuia Impetiginosa, Astragalus Menziesii, Propolis, Glandula Suprarenalis Suis, Thymus (suis), Aranea Diadema, Gelsemium Sempervirens, Ipecacuanha, Lycopodium Clavatum, Mercurius Solubilis, Muriaticum Acidum, Nitricum Acidum, Rhus Toxicodendron, Selenium Metallicum, Silicea, Epstein Barr Virus</NonProprietaryName></NDC></NDCList>