{
"NDC": [
{
"NDCCode": "62902-0012-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0012-1) ",
"NDC11Code": "62902-0012-01",
"ProductNDC": "62902-0012",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Hormone Harmony",
"NonProprietaryName": "Salsolinol (hydrochloride), Dhea (dehydroepiandrosterone), 7-oxo- Dehydroepiandrosterone-3b-acetate (7-keto), Cholesterinum, Folliculinum, Oophorinum (suis), Progesterone, Testosterone, Cortisone Aceticum, Aldosterone, Androsterone, Follicle Stimulating Hormone",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20181022",
"EndMarketingDate": "20231212",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": "7-OXODEHYDROEPIANDROSTERONE 3-ACETATE; ALDOSTERONE; ANDROSTERONE; CHOLESTEROL; CORTISONE ACETATE; ESTRONE; FOLLITROPIN; PRASTERONE; PROGESTERONE; SALSOLINOL HYDROCHLORIDE, (+/-)-; SUS SCROFA OVARY; TESTOSTERONE",
"StrengthNumber": "8; 12; 12; 8; 12; 8; 12; 6; 8; 6; 8; 8",
"StrengthUnit": "[hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Pharm_Classes": "Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Gonadotropin [EPC], Gonadotropins [CS], Progesterone [CS], Progesterone [EPC]",
"DEASchedule": "CIII",
"Status": "Deprecated",
"LastUpdate": "2023-12-13",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20181022",
"EndMarketingDatePackage": "20231212",
"SamplePackage": "N"
},
{
"NDCCode": "62902-0001-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0001-1)",
"NDC11Code": "62902-0001-01",
"ProductNDC": "62902-0001",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Lean Love",
"NonProprietaryName": "Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Brain (suis), Hepar Suis, Methylcobalamin, Pancreas Suis, Kidney (suis), Stomach (suis), Aacg-a, Aacg-b, Calcarea Carbonica, Gambogia Gelsemium, Sempervirens Graphites, Nux Vomica, Phytolacca Decandra, 7-keto-dhea (dehydroepiandrosterone), Atp (adenosinum Triphosphoricum Dinatrum), Glucagon, Insulinum, Sarcolacticum Acidum, Proteus (vulgaris)",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20140522",
"EndMarketingDate": "20190513",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": "CYNANCHUM VINCETOXICUM ROOT; ECHINACEA ANGUSTIFOLIA; SUS SCROFA HYPOTHALAMUS; PORK BRAIN; PORK LIVER; METHYLCOBALAMIN; SUS SCROFA PANCREAS; PORK KIDNEY; SUS SCROFA STOMACH; APC-356433; APC-356434; OYSTER SHELL CALCIUM CARBONATE, CRUDE; GAMBOGE; GELSEMIUM SEMPERVIRENS ROOT; GRAPHITE; STRYCHNOS NUX-VOMICA SEED; PHYTOLACCA AMERICANA ROOT; 7-KETO-DEHYDROEPIANDROSTERONE; ADENOSINE TRIPHOSPHATE DISODIUM; GLUCAGON; INSULIN HUMAN; LACTIC ACID, L-; PROTEUS VULGARIS",
"StrengthNumber": "6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 12; 12; 12; 12; 12; 12; 30; 30; 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_C]/mL",
"Status": "Deprecated",
"LastUpdate": "2019-05-14",
"ProductNdcExcludeFlag": "N"
},
{
"NDCCode": "62902-0002-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0002-1) ",
"NDC11Code": "62902-0002-01",
"ProductNDC": "62902-0002",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Craving And Appetite Ease",
"NonProprietaryName": "Acetyl Coenzyme A, Adenosinum Triphosphoricum Dinatrum, Adrenal Cortex (suis), Bacopa Speciosa, Dopamine Hydrochloride, Equol, Gambogia, Oxytocin Acetate, Rhodiola, Stomach (suis), Thyroidinum (suis), Chininum Sulphuricum, Cina, Iodium, Lycopodium Clavatum, Phosphorus, Serotonin (hydrochloride), Morgan Gaertner",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20160824",
"EndMarketingDate": "20220602",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": "ACETYL COENZYME A; ADENOSINE TRIPHOSPHATE DISODIUM; ARTEMISIA CINA PRE-FLOWERING TOP; BACOPA MONNIERI WHOLE; DOPAMINE HYDROCHLORIDE; EQUOL, (+/-)-; GAMBOGE; IODINE; LYCOPODIUM CLAVATUM SPORE; OXYTOCIN ACETATE; PHOSPHORUS; QUININE SULFATE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; SEDUM ROSEUM WHOLE; SEROTONIN HYDROCHLORIDE; SUS SCROFA ADRENAL CORTEX; SUS SCROFA STOMACH; SUS SCROFA THYROID",
"StrengthNumber": "6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 30; 6; 6; 6; 6; 6",
"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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Pharm_Classes": "Antimalarial [EPC], Catecholamine [EPC], Catecholamines [CS], Increased Uterine Smooth Muscle Contraction or Tone [PE], Oxytocic [EPC], Oxytocin [CS]",
"Status": "Deprecated",
"LastUpdate": "2022-06-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20160824",
"EndMarketingDatePackage": "20220602",
"SamplePackage": "N"
},
{
"NDCCode": "62902-0003-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0003-1) ",
"NDC11Code": "62902-0003-01",
"ProductNDC": "62902-0003",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Metabolic Rewire Support",
"NonProprietaryName": "Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Hepar Suis, Kidney (suis), Methylcobalamin, Gambogia, Graphites, Nux Vomica, Phytolacca Decandra, 7-keto (3-acetyl-7-oxo-dehydroepiandrosterone), Adenosinum Triphosphoricum Dinatrum, Glucagon, Insulinum (suis), Sarcolacticum Acidum, Proteus (vulgaris)",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20151012",
"EndMarketingDate": "20220602",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": "7-KETO-DEHYDROEPIANDROSTERONE; ADENOSINE TRIPHOSPHATE DISODIUM; CYNANCHUM VINCETOXICUM ROOT; ECHINACEA ANGUSTIFOLIA; GAMBOGE; GLUCAGON; GRAPHITE; INSULIN PORK; LACTIC ACID, L-; METHYLCOBALAMIN; PHYTOLACCA AMERICANA ROOT; PORK KIDNEY; PORK LIVER; PROTEUS VULGARIS; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA HYPOTHALAMUS",
"StrengthNumber": "30; 30; 6; 6; 12; 30; 12; 30; 30; 8; 12; 8; 8; 30; 12; 6",
"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_C]/mL; [hp_X]/mL; [hp_X]/mL",
"Pharm_Classes": "Allergens [CS], Antihypoglycemic Agent [EPC], Cell-mediated Immunity [PE], Decreased GI Motility [PE], Decreased GI Smooth Muscle Tone [PE], Decreased Glycolysis [PE], Gastrointestinal Motility Inhibitor [EPC], Increased Gluconeogenesis [PE], Increased Glycogenolysis [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]",
"Status": "Deprecated",
"LastUpdate": "2022-06-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20151012",
"EndMarketingDatePackage": "20220602",
"SamplePackage": "N"
},
{
"NDCCode": "62902-0004-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0004-1) ",
"NDC11Code": "62902-0004-01",
"ProductNDC": "62902-0004",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Hgh Vibrancy",
"NonProprietaryName": "Agnus Castus, Ambra Grisea, Conium Maculatum, Apiolum, Estradiol, Estriol, Folliculinum, L-dopa, Melatonin, Testosterone, Alpha-lipoicum Acidum, Adenosinum Triphosphoricum Dinatrum, Coenzyme A, Ubidecarenonum, Nadidum, Sarcolacticum Acidum, Baryta Carbonica, Selenium Metallicum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (suis), Lymph Node(suis), Medulla Ossis Suis, Oophorinum (suis), Orchitinum (suis), Pancreas Suis, Spleen (suis)",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20151012",
"EndMarketingDate": "20201026",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": "CHASTE TREE; AMBERGRIS; CONIUM MACULATUM FLOWERING TOP; APIOLE (PARSLEY); ESTRADIOL; ESTRIOL; ESTRONE; LEVODOPA; MELATONIN; TESTOSTERONE; ADENOSINE TRIPHOSPHATE DISODIUM; .ALPHA.-LIPOIC ACID; COENZYME A; NADIDE; LACTIC ACID, L-; UBIDECARENONE; BARIUM CARBONATE; SELENIUM; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; PORK LIVER; SUS SCROFA HYPOTHALAMUS; SUS SCROFA LYMPH; SUS SCROFA BONE MARROW; SUS SCROFA OVARY; SUS SCROFA TESTICLE; SUS SCROFA PANCREAS; SUS SCROFA SPLEEN; SOMATROPIN; PROTEUS MORGANII",
"StrengthNumber": "6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 30; 30; 30; 30; 30; 30; 30; 30; 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_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2020-10-29",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20151012",
"EndMarketingDatePackage": "20201026",
"SamplePackage": "N"
},
{
"NDCCode": "62902-0005-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0005-1) ",
"NDC11Code": "62902-0005-01",
"ProductNDC": "62902-0005",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Clean Sweep Formula 1",
"NonProprietaryName": "Acetylcholine Chloride, Adrenalinum, Dopamine Hydrochloride, Gaba, Norepinephrine, Octopamine (hydrochloride), Serotonin (hydrochloride), Taurine, Adenosinum Cyclophosphoricum, Cerebrum (suis), Diencephalon (suis), Pineal Gland (suis), Thalamus Opticus,",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20170509",
"EndMarketingDate": "20220602",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": ".GAMMA.-AMINOBUTYRIC ACID; ACETYLCHOLINE CHLORIDE; ADENOSINE CYCLIC PHOSPHATE; DOPAMINE HYDROCHLORIDE; EPINEPHRINE; NOREPINEPHRINE; OCTOPAMINE HYDROCHLORIDE; SEROTONIN HYDROCHLORIDE; SUS SCROFA CEREBRUM; SUS SCROFA DIENCEPHALON; SUS SCROFA PINEAL GLAND; SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS; TAURINE",
"StrengthNumber": "6; 6; 8; 6; 6; 6; 6; 6; 8; 8; 8; 8; 6",
"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",
"Pharm_Classes": "Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Catecholamine [EPC], Catecholamine [EPC], Catecholamine [EPC], Catecholamines [CS], Catecholamines [CS], Catecholamines [CS], Cholinergic Agonists [MoA], Cholinergic Receptor Agonist [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]",
"Status": "Deprecated",
"LastUpdate": "2022-06-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20170509",
"EndMarketingDatePackage": "20220602",
"SamplePackage": "N"
},
{
"NDCCode": "62902-0006-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0006-1) ",
"NDC11Code": "62902-0006-01",
"ProductNDC": "62902-0006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Clean Sweep Formula 2",
"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, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Gnaphalium Polycephalum",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20170510",
"EndMarketingDate": "20220602",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": "AMMONIUM CHLORIDE; BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC ACETATE; ENTEROBACTER CLOACAE; HORSE CHESTNUT; MERCURIC OXIDE; NADIDE; NIACINAMIDE; PANTOTHENIC ACID; PICRIC ACID; PROTEUS MORGANII; PROTEUS VULGARIS; PSEUDOGNAPHALIUM OBTUSIFOLIUM; PYRIDOXINE HYDROCHLORIDE; RANUNCULUS BULBOSUS; RHODODENDRON TOMENTOSUM LEAFY TWIG; RIBOFLAVIN; SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS; SILICON DIOXIDE; SILVER; SODIUM DIETHYL OXALACETATE; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA BONE MARROW; SUS SCROFA CARTILAGE; SUS SCROFA INTERVERTEBRAL DISC; SUS SCROFA UMBILICAL CORD; THIAMINE HYDROCHLORIDE; THIOCTIC ACID; TRIBASIC CALCIUM PHOSPHATE",
"StrengthNumber": "8; 4; 4; 4; 4; 6; 30; 6; 10; 6; 6; 10; 6; 30; 30; 10; 6; 4; 4; 6; 30; 8; 10; 6; 28; 10; 10; 8; 8; 10; 6; 8; 10",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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": "Analogs/Derivatives [Chemical/Ingredient], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC]",
"Status": "Deprecated",
"LastUpdate": "2022-06-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20170510",
"EndMarketingDatePackage": "20220602",
"SamplePackage": "N"
},
{
"NDCCode": "62902-0007-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0007-1) ",
"NDC11Code": "62902-0007-01",
"ProductNDC": "62902-0007",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Clean Sweep Formula 3",
"NonProprietaryName": "Ceanothus Americanus, Veratrum Album, Anacardium Orientale, Argentum Nitricum, Condurango, Hydrastis Canadensis, Momordica Balsamina, Oxalis Acetosella, Pulsatilla (vulgaris), 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, Rectal Mucosa (suis), Stomach (suis)",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20170510",
"EndMarketingDate": "20220602",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": "ANEMONE PULSATILLA; ATROPA BELLADONNA; CEANOTHUS AMERICANUS LEAF; GOLDENSEAL; IPECAC; LACHESIS MUTA VENOM; MANDRAGORA OFFICINARUM ROOT; MARSDENIA CONDURANGO BARK; MOMORDICA BALSAMINA IMMATURE FRUIT; OXALIS ACETOSELLA LEAF; PHOSPHORUS; PORK INTESTINE; POTASSIUM DICHROMATE; SEMECARPUS ANACARDIUM JUICE; SHIGELLA DYSENTERIAE; SILVER NITRATE; SODIUM DIETHYL OXALACETATE; SULFUR; SUS SCROFA BILE DUCT; SUS SCROFA COLON; SUS SCROFA DUODENUM; SUS SCROFA ESOPHAGUS; SUS SCROFA EYE; SUS SCROFA GALLBLADDER; SUS SCROFA ILEUM; SUS SCROFA JEJUNUM; SUS SCROFA LUNG; SUS SCROFA NASAL MUCOSA; SUS SCROFA ORAL MUCOSA; SUS SCROFA PANCREAS; SUS SCROFA RECTAL MUCOSA; SUS SCROFA STOMACH; SUS SCROFA URINARY BLADDER; VERATRUM ALBUM ROOT; WOOD CREOSOTE; YEAST MANNAN",
"StrengthNumber": "6; 8; 4; 6; 8; 10; 10; 6; 6; 6; 8; 8; 8; 6; 30; 6; 8; 8; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 6; 4; 10; 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_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_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; [hp_X]/mL; [hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2022-06-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20170510",
"EndMarketingDatePackage": "20220602",
"SamplePackage": "N"
},
{
"NDCCode": "62902-0008-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0008-1) ",
"NDC11Code": "62902-0008-01",
"ProductNDC": "62902-0008",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Clean Sweep Formula 4",
"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, Alpha-ketoglutaricum Acidum, Cholesterinum, Formicum Acidum, Glyoxal Trimer Dihydrate, Histaminum Hydrochloricum, Malicum Acidum, Natrum Oxalaceticum, Sulphur, Calcarea Carbonica",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20170511",
"EndMarketingDate": "20220601",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": "AVENA SATIVA FLOWERING TOP; CHELIDONIUM MAJUS; CHOLESTEROL; CINCHONA OFFICINALIS BARK; CYNARA SCOLYMUS LEAF; FORMIC ACID; GLYOXAL TRIMER DIHYDRATE; HISTAMINE DIHYDROCHLORIDE; LYCOPODIUM CLAVATUM SPORE; MALIC ACID; MENADIONE; METHYLCOBALAMIN; MILK THISTLE; OROTIC ACID; OXOGLURIC ACID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PORK INTESTINE; PORK LIVER; PROTEUS MORGANII; SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS; SODIUM DIETHYL OXALACETATE; SULFUR; SUS SCROFA COLON; SUS SCROFA DUODENUM; SUS SCROFA GALLBLADDER; SUS SCROFA LYMPH; SUS SCROFA PANCREAS; SUS SCROFA THYMUS; TARAXACUM OFFICINALE; THIOCTIC ACID; VERATRUM ALBUM ROOT",
"StrengthNumber": "6; 4; 10; 4; 6; 10; 10; 10; 4; 10; 6; 6; 3; 7; 10; 28; 8; 8; 30; 30; 10; 13; 8; 8; 8; 8; 8; 8; 4; 8; 4",
"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_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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": "2022-06-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20170511",
"EndMarketingDatePackage": "20220601",
"SamplePackage": "N"
},
{
"NDCCode": "62902-0009-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0009-1) ",
"NDC11Code": "62902-0009-01",
"ProductNDC": "62902-0009",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Clean Sweep Formula 5",
"NonProprietaryName": "Solidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, Equisetum Hyemale, Argentum Nitricum, Cantharis, Capsicum Annuum, Cuprum Sulphuricum, Orthosiphon Stamineus, Pareira Brava, Sarsaparilla (smilax Regelii), Terebinthina, Apis Venenum Purum, Barosma (betulina), 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": "20170512",
"EndMarketingDate": "20220601",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": "AGATHOSMA BETULINA LEAF; APIS MELLIFERA VENOM; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; CALCIUM SULFIDE; CAPSICUM; CHONDRODENDRON TOMENTOSUM ROOT; CUPRIC SULFATE; EQUISETUM HYEMALE; ESCHERICHIA COLI; GLYOXAL TRIMER DIHYDRATE; LYTTA VESICATORIA; MERCURIC CHLORIDE; QUERCETIN; SHIGELLA DYSENTERIAE; SILVER NITRATE; SMILAX ORNATA ROOT; SODIUM PYRUVATE; SOLIDAGO VIRGAUREA FLOWERING TOP; SUS SCROFA RENAL PELVIS; SUS SCROFA URETER; SUS SCROFA URETHRA; SUS SCROFA URINARY BLADDER; TURPENTINE OIL",
"StrengthNumber": "8; 8; 4; 4; 10; 6; 6; 6; 4; 15; 8; 6; 8; 10; 30; 6; 6; 10; 3; 8; 8; 8; 8; 6",
"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_C]/mL; [hp_X]/mL; [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], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]",
"Status": "Deprecated",
"LastUpdate": "2022-06-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20170512",
"EndMarketingDatePackage": "20220601",
"SamplePackage": "N"
},
{
"NDCCode": "62902-0010-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0010-1) ",
"NDC11Code": "62902-0010-01",
"ProductNDC": "62902-0010",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Clean Sweep Formula 6",
"NonProprietaryName": "Conium Maculatum, Dulcamara, Echinacea (angustifolia), Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbic Acid, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Pulsatilla (vulgaris), Sarcolacticum Acidum, Lymph Node (suis), Sulphur, Glandula Suprarenalis Suis, L-phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus (suis), Spleen (suis), Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Glyphosate, Funiculus Umbilicalis Suis",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20170512",
"EndMarketingDate": "20220601",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": "ANTIMONY POTASSIUM TARTRATE; ASCORBIC ACID; BARIUM CARBONATE; BISPHENOL A; BROMINE; CHLORINE; CONIUM MACULATUM FLOWERING TOP; CORTISONE ACETATE; ECHINACEA ANGUSTIFOLIA; ESCHERICHIA COLI; FERRUM PHOSPHORICUM; GALIUM APARINE; GENTIANA LUTEA ROOT; GLYPHOSATE; HORSE CHESTNUT; HYDROFLUORIC ACID; IODINE; LACTIC ACID, L-; LIOTHYRONINE; MERCURIUS SOLUBILIS; PHENYLALANINE; PORK LIVER; PROTORTONIA CACTI; PULSATILLA VULGARIS; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; SOLANUM DULCAMARA TOP; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA BONE MARROW; SUS SCROFA HYPOTHALAMUS; SUS SCROFA LYMPH; SUS SCROFA SPLEEN; SUS SCROFA TONSIL; SUS SCROFA UMBILICAL CORD; TRIBASIC CALCIUM PHOSPHATE",
"StrengthNumber": "6; 6; 28; 12; 12; 12; 4; 13; 4; 30; 10; 6; 6; 1000; 6; 12; 12; 6; 10; 13; 8; 10; 6; 6; 9; 4; 8; 8; 12; 10; 6; 10; 6; 6; 10",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL",
"Pharm_Classes": "Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Increased Coagulation Factor Activity [PE], Triiodothyronine [CS], Vitamin C [EPC], l-Triiodothyronine [EPC]",
"Status": "Deprecated",
"LastUpdate": "2022-06-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20170512",
"EndMarketingDatePackage": "20220601",
"SamplePackage": "N"
},
{
"NDCCode": "62902-0011-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0011-1) ",
"NDC11Code": "62902-0011-01",
"ProductNDC": "62902-0011",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Lean Love",
"NonProprietaryName": "Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Cerebrum Suis, Hepar Suis, Methylcobalamin, Pancreas Suis, Kidney (suis), Stomach (suis), Aacg-a, Aacg-b, Calcarea Carbonica, Gambogia Gelsemium, Sempervirens Graphites, Nux Vomica, Phytolacca Decandra, 7-keto (3-acetyl-7-oxo-dehyroepiandrosterone), Adenosinum Triphosphoricum Dinatrum, Glucagon, Insulinum (suis), Sarcolacticum Acidum, Proteus (vulgaris)",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20170509",
"EndMarketingDate": "20220607",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": "7-KETO-DEHYDROEPIANDROSTERONE; ADENOSINE TRIPHOSPHATE DISODIUM; APC-356433; APC-356434; CYNANCHUM VINCETOXICUM ROOT; ECHINACEA ANGUSTIFOLIA; GAMBOGE; GELSEMIUM SEMPERVIRENS ROOT; GLUCAGON; GRAPHITE; INSULIN PORK; LACTIC ACID, L-; METHYLCOBALAMIN; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; PORK KIDNEY; PORK LIVER; PROTEUS VULGARIS; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA CEREBRUM; SUS SCROFA HYPOTHALAMUS; SUS SCROFA PANCREAS; SUS SCROFA STOMACH",
"StrengthNumber": "30; 30; 8; 8; 6; 6; 12; 12; 30; 12; 30; 30; 8; 12; 12; 8; 8; 30; 12; 8; 6; 8; 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_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL",
"Pharm_Classes": "Allergens [CS], Antihypoglycemic Agent [EPC], Cell-mediated Immunity [PE], Decreased GI Motility [PE], Decreased GI Smooth Muscle Tone [PE], Decreased Glycolysis [PE], Gastrointestinal Motility Inhibitor [EPC], Increased Gluconeogenesis [PE], Increased Glycogenolysis [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]",
"Status": "Deprecated",
"LastUpdate": "2022-06-08",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20170509",
"EndMarketingDatePackage": "20220607",
"SamplePackage": "N"
},
{
"NDCCode": "62902-0013-1",
"PackageDescription": "30 mL in 1 BOTTLE, DROPPER (62902-0013-1) ",
"NDC11Code": "62902-0013-01",
"ProductNDC": "62902-0013",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Hgh Vibrancy",
"NonProprietaryName": "Agnus Castus, Ambra Grisea, Conium Maculatum, Apiolum, Estradiol, Estriol, Folliculinum, L-dopa, Melatonin, Testosterone, Alpha-lipoicum Acidum, Adenosinum Triphosphoricum Dinatrum, Ubidecarenonum, Nadidum, Sarcolacticum Acidum, Baryta Carbonica, Selenium Metallicum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (suis), Lymph Node(suis), Medulla Ossis Suis, Oophorinum (suis), Orchitinum (suis), Pancreas Suis, Spleen (suis), Human Growth Hormone, Proteus (morgani)",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20181105",
"EndMarketingDate": "20240111",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Intentional Nourishment",
"SubstanceName": ".ALPHA.-LIPOIC ACID; ADENOSINE TRIPHOSPHATE DISODIUM; AMBERGRIS; APIOLE (PARSLEY); BARIUM CARBONATE; CHASTE TREE; CONIUM MACULATUM FLOWERING TOP; ESTRADIOL; ESTRIOL; ESTRONE; LACTIC ACID, L-; LEVODOPA; MELATONIN; NADIDE; PANTOTHENIC ACID; PORK LIVER; PROTEUS MORGANII; SELENIUM; SOMATROPIN; SUS SCROFA ADRENAL GLAND; SUS SCROFA BONE MARROW; SUS SCROFA HYPOTHALAMUS; SUS SCROFA LYMPH; SUS SCROFA OVARY; SUS SCROFA PANCREAS; SUS SCROFA SPLEEN; SUS SCROFA TESTICLE; SUS SCROFA UMBILICAL CORD; TESTOSTERONE; UBIDECARENONE",
"StrengthNumber": "8; 8; 6; 6; 8; 6; 8; 6; 6; 8; 8; 6; 6; 8; 8; 30; 30; 8; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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": "Amino Acids, Aromatic [CS], Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Aromatic Amino Acid [EPC], Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Human Growth Hormone [CS], Recombinant Human Growth Hormone [EPC]",
"DEASchedule": "CIII",
"Status": "Deprecated",
"LastUpdate": "2024-01-12",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20181105",
"EndMarketingDatePackage": "20240111",
"SamplePackage": "N",
"IndicationAndUsage": "For the temporary relief of symptoms related to aging including fatigue, minor joint pain and muscle soreness.**. **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration."
},
{
"NDCCode": "0009-0012-01",
"PackageDescription": "50 TABLET in 1 BOTTLE (0009-0012-01) ",
"NDC11Code": "00009-0012-01",
"ProductNDC": "0009-0012",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Cortef",
"NonProprietaryName": "Hydrocortisone",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "19521215",
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA008697",
"LabelerName": "Pharmacia & Upjohn Company LLC",
"SubstanceName": "HYDROCORTISONE",
"StrengthNumber": "5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]",
"Status": "Active",
"LastUpdate": "2025-02-20",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "19521215",
"SamplePackage": "N",
"IndicationAndUsage": "CORTEF Tablets are indicated in the following conditions.",
"Description": "CORTEF Tablets contain hydrocortisone which is a glucocorticoid. Glucocorticoids are adrenocortical steroids, both naturally occurring and synthetic, which are readily absorbed from the gastrointestinal tract. Hydrocortisone USP is white to practically white, odorless, crystalline powder with a melting point of about 215° C. It is very slightly soluble in water and in ether; sparingly soluble in acetone and in alcohol; slightly soluble in chloroform. The chemical name for hydrocortisone is pregn-4-ene-3,20-dione,11,17,21-trihydroxy-, (11β)-. Its molecular weight is 362.46 and the structural formula is as outlined below. CORTEF Tablets are available for oral administration in three strengths: each tablet contains either 5 mg, 10 mg, or 20 mg of hydrocortisone. Inactive ingredients: calcium stearate, corn starch, lactose, mineral oil, sorbic acid, sucrose."
},
{
"NDCCode": "0054-0012-20",
"PackageDescription": "100 BLISTER PACK in 1 CARTON (0054-0012-20) / 1 TABLET in 1 BLISTER PACK",
"NDC11Code": "00054-0012-20",
"ProductNDC": "0054-0012",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Flecainide Acetate",
"NonProprietaryName": "Flecainide Acetate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20030114",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076278",
"LabelerName": "Hikma Pharmaceuticals USA Inc.",
"SubstanceName": "FLECAINIDE ACETATE",
"StrengthNumber": "150",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Antiarrhythmic [EPC]",
"Status": "Active",
"LastUpdate": "2024-12-06",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20030114",
"SamplePackage": "N",
"IndicationAndUsage": "In patients without structural heart disease, flecainide acetate is indicated for the prevention of: 1 paroxysmal supraventricular tachycardias (PSVT), including atrioventricular nodal reentrant tachycardia, atrioventricular reentrant tachycardia and other supraventricular tachycardias of unspecified mechanism associated with disabling symptoms, 2 paroxysmal atrial fibrillation/flutter (PAF) associated with disabling symptoms.",
"Description": "Flecainide Acetate Tablets, USP are an antiarrhythmic drug containing 50 mg, 100 mg or 150 mg of flecainide acetate, USP for oral administration. Flecainide acetate is N-(2-piperidylmethyl)-2,5-bis(2,2,2-trifluoroethoxy)benzamide monoacetate. The structural formula is given below. : 1 ."
},
{
"NDCCode": "0054-0012-21",
"PackageDescription": "60 TABLET in 1 BOTTLE (0054-0012-21) ",
"NDC11Code": "00054-0012-21",
"ProductNDC": "0054-0012",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Flecainide Acetate",
"NonProprietaryName": "Flecainide Acetate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20030114",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076278",
"LabelerName": "Hikma Pharmaceuticals USA Inc.",
"SubstanceName": "FLECAINIDE ACETATE",
"StrengthNumber": "150",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Antiarrhythmic [EPC]",
"Status": "Active",
"LastUpdate": "2024-12-06",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20030114",
"SamplePackage": "N",
"IndicationAndUsage": "In patients without structural heart disease, flecainide acetate is indicated for the prevention of: 1 paroxysmal supraventricular tachycardias (PSVT), including atrioventricular nodal reentrant tachycardia, atrioventricular reentrant tachycardia and other supraventricular tachycardias of unspecified mechanism associated with disabling symptoms, 2 paroxysmal atrial fibrillation/flutter (PAF) associated with disabling symptoms.",
"Description": "Flecainide Acetate Tablets, USP are an antiarrhythmic drug containing 50 mg, 100 mg or 150 mg of flecainide acetate, USP for oral administration. Flecainide acetate is N-(2-piperidylmethyl)-2,5-bis(2,2,2-trifluoroethoxy)benzamide monoacetate. The structural formula is given below. : 1 ."
},
{
"NDCCode": "0054-0012-25",
"PackageDescription": "100 TABLET in 1 BOTTLE (0054-0012-25) ",
"NDC11Code": "00054-0012-25",
"ProductNDC": "0054-0012",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Flecainide Acetate",
"NonProprietaryName": "Flecainide Acetate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20030114",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076278",
"LabelerName": "Hikma Pharmaceuticals USA Inc.",
"SubstanceName": "FLECAINIDE ACETATE",
"StrengthNumber": "150",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Antiarrhythmic [EPC]",
"Status": "Active",
"LastUpdate": "2024-12-06",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20030114",
"SamplePackage": "N",
"IndicationAndUsage": "In patients without structural heart disease, flecainide acetate is indicated for the prevention of: 1 paroxysmal supraventricular tachycardias (PSVT), including atrioventricular nodal reentrant tachycardia, atrioventricular reentrant tachycardia and other supraventricular tachycardias of unspecified mechanism associated with disabling symptoms, 2 paroxysmal atrial fibrillation/flutter (PAF) associated with disabling symptoms.",
"Description": "Flecainide Acetate Tablets, USP are an antiarrhythmic drug containing 50 mg, 100 mg or 150 mg of flecainide acetate, USP for oral administration. Flecainide acetate is N-(2-piperidylmethyl)-2,5-bis(2,2,2-trifluoroethoxy)benzamide monoacetate. The structural formula is given below. : 1 ."
},
{
"NDCCode": "0093-0012-98",
"PackageDescription": "90 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-0012-98) ",
"NDC11Code": "00093-0012-98",
"ProductNDC": "0093-0012",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Pantoprazole Sodium",
"NonProprietaryName": "Pantoprazole Sodium",
"DosageFormName": "TABLET, DELAYED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20071219",
"EndMarketingDate": "20200531",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077056",
"LabelerName": "Teva Pharmaceuticals USA, Inc.",
"SubstanceName": "PANTOPRAZOLE SODIUM",
"StrengthNumber": "40",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]",
"Status": "Deprecated",
"LastUpdate": "2020-06-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20071219",
"EndMarketingDatePackage": "20200531",
"SamplePackage": "N"
},
{
"NDCCode": "0168-0012-09",
"PackageDescription": "144 PACKET in 1 CARTON (0168-0012-09) > .9 g in 1 PACKET",
"NDC11Code": "00168-0012-09",
"ProductNDC": "0168-0012",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Triple Antibiotic",
"NonProprietaryName": "Neomycin And Polymyxin B Sulfates And Bacitracin Zinc",
"DosageFormName": "OINTMENT",
"RouteName": "TOPICAL",
"StartMarketingDate": "20100106",
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part333B",
"LabelerName": "E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.",
"SubstanceName": "BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE",
"StrengthNumber": "400; 3.5; 5000",
"StrengthUnit": "[USP'U]/g; mg/g; [USP'U]/g",
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20181231"
},
{
"NDCCode": "0168-0012-31",
"PackageDescription": "1 TUBE in 1 CARTON (0168-0012-31) > 28.35 g in 1 TUBE",
"NDC11Code": "00168-0012-31",
"ProductNDC": "0168-0012",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Triple Antibiotic",
"NonProprietaryName": "Neomycin And Polymyxin B Sulfates And Bacitracin Zinc",
"DosageFormName": "OINTMENT",
"RouteName": "TOPICAL",
"StartMarketingDate": "20100106",
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part333B",
"LabelerName": "E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.",
"SubstanceName": "BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE",
"StrengthNumber": "400; 3.5; 5000",
"StrengthUnit": "[USP'U]/g; mg/g; [USP'U]/g",
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20181231"
},
{
"NDCCode": "0168-0012-35",
"PackageDescription": "1 TUBE in 1 CARTON (0168-0012-35) > 14.17 g in 1 TUBE",
"NDC11Code": "00168-0012-35",
"ProductNDC": "0168-0012",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Triple Antibiotic",
"NonProprietaryName": "Neomycin And Polymyxin B Sulfates And Bacitracin Zinc",
"DosageFormName": "OINTMENT",
"RouteName": "TOPICAL",
"StartMarketingDate": "20100106",
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part333B",
"LabelerName": "E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.",
"SubstanceName": "BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE",
"StrengthNumber": "400; 3.5; 5000",
"StrengthUnit": "[USP'U]/g; mg/g; [USP'U]/g",
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20181231"
},
{
"NDCCode": "0187-0011-10",
"PackageDescription": "1 KIT in 1 PACKAGE (0187-0011-10) * 10 TRAY in 1 PACKAGE > 1 VIAL, SINGLE-DOSE in 1 TRAY > .5 mL in 1 VIAL, SINGLE-DOSE * .6 mL in 1 SYRINGE (0187-0012-01) ",
"NDC11Code": "00187-0011-10",
"ProductNDC": "0187-0011",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Iprivask",
"NonProprietaryName": "Desirudin",
"DosageFormName": "KIT",
"StartMarketingDate": "20131231",
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA021271",
"LabelerName": "Valeant Pharmaceuticals North America LLC",
"Status": "Deprecated",
"LastUpdate": "2018-10-04",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20131231",
"SamplePackage": "N"
},
{
"NDCCode": "0220-0012-11",
"PackageDescription": "30 mL in 1 BOTTLE, GLASS (0220-0012-11)",
"NDC11Code": "00220-0012-11",
"ProductNDC": "0220-0012",
"ProductTypeName": "DRUG FOR FURTHER PROCESSING",
"NonProprietaryName": "Artemisia Abrotanum Flowering Top",
"DosageFormName": "PELLET",
"StartMarketingDate": "20170101",
"MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
"LabelerName": "Laboratoires Boiron",
"SubstanceName": "ARTEMISIA ABROTANUM FLOWERING TOP",
"StrengthNumber": "1",
"StrengthUnit": "[hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2014-02-04",
"ListingRecordCertifiedThrough": "20181231"
},
{
"NDCCode": "0220-0012-12",
"PackageDescription": "60 mL in 1 BOTTLE, GLASS (0220-0012-12)",
"NDC11Code": "00220-0012-12",
"ProductNDC": "0220-0012",
"ProductTypeName": "DRUG FOR FURTHER PROCESSING",
"NonProprietaryName": "Artemisia Abrotanum Flowering Top",
"DosageFormName": "PELLET",
"StartMarketingDate": "20170101",
"MarketingCategoryName": "DRUG FOR FURTHER PROCESSING",
"LabelerName": "Laboratoires Boiron",
"SubstanceName": "ARTEMISIA ABROTANUM FLOWERING TOP",
"StrengthNumber": "1",
"StrengthUnit": "[hp_X]/mL",
"Status": "Deprecated",
"LastUpdate": "2014-02-04",
"ListingRecordCertifiedThrough": "20181231"
},
{
"NDCCode": "0245-0012-01",
"PackageDescription": "100 BLISTER PACK in 1 CARTON (0245-0012-01) / 1 TABLET in 1 BLISTER PACK (0245-0012-89) ",
"NDC11Code": "00245-0012-01",
"ProductNDC": "0245-0012",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Sorine",
"NonProprietaryName": "Sotalol Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20110215",
"EndMarketingDate": "20250131",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA075500",
"LabelerName": "Upsher-Smith Laboratories, Inc.",
"SubstanceName": "SOTALOL HYDROCHLORIDE",
"StrengthNumber": "80",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Adrenergic beta-Antagonists [MoA], Antiarrhythmic [EPC], Cardiac Rhythm Alteration [PE]",
"Status": "Deprecated",
"LastUpdate": "2024-06-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20110215",
"EndMarketingDatePackage": "20240531",
"SamplePackage": "N",
"IndicationAndUsage": "SORINE (sotalol hydrochloride) is an antiarrhythmic indicated for: 1 the treatment of life-threatening ventricular arrhythmias (1.1), 2 the maintenance of normal sinus rhythm in patients with atrial fibrillation or flutter (AFIB/AFL) (1.2).",
"Description": "SORINE contains sotalol hydrochloride, USP an antiarrhythmic drug with Class II (beta-adrenoreceptor blocking) and Class III (cardiac action potential duration prolongation) properties. SORINE (sotalol hydrochloride, USP) is supplied as a white, capsule-shaped tablet for oral administration. Sotalol hydrochloride, USP is a white, crystalline solid with a molecular weight of 308.8. It is hydrophilic, soluble in water, propylene glycol and ethanol, but is only slightly soluble in chloroform. Chemically, sotalol hydrochloride, USP is d,l-N-[4-[1-hydroxy-2-[(1-methylethyl) amino]ethyl]phenyl]methane-sulfonamide monohydrochloride. The molecular formula is C12H20N2O3 S∙HCl and is represented by the following structural formula. SORINE Tablets contain the following inactive ingredients: microcrystalline cellulose, lactose monohydrate, corn starch, stearic acid, magnesium stearate and silicon dioxide."
},
{
"NDCCode": "0245-0012-11",
"PackageDescription": "100 TABLET in 1 BOTTLE (0245-0012-11) ",
"NDC11Code": "00245-0012-11",
"ProductNDC": "0245-0012",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Sorine",
"NonProprietaryName": "Sotalol Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20110215",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA075500",
"LabelerName": "Upsher-Smith Laboratories, Inc.",
"SubstanceName": "SOTALOL HYDROCHLORIDE",
"StrengthNumber": "80",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Adrenergic beta-Antagonists [MoA], Antiarrhythmic [EPC], Cardiac Rhythm Alteration [PE]",
"Status": "Deprecated",
"LastUpdate": "2024-01-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20110215",
"SamplePackage": "N",
"IndicationAndUsage": "SORINE (sotalol hydrochloride) is an antiarrhythmic indicated for: 1 the treatment of life-threatening ventricular arrhythmias (1.1), 2 the maintenance of normal sinus rhythm in patients with atrial fibrillation or flutter (AFIB/AFL) (1.2).",
"Description": "SORINE contains sotalol hydrochloride, USP an antiarrhythmic drug with Class II (beta-adrenoreceptor blocking) and Class III (cardiac action potential duration prolongation) properties. SORINE (sotalol hydrochloride, USP) is supplied as a white, capsule-shaped tablet for oral administration. Sotalol hydrochloride, USP is a white, crystalline solid with a molecular weight of 308.8. It is hydrophilic, soluble in water, propylene glycol and ethanol, but is only slightly soluble in chloroform. Chemically, sotalol hydrochloride, USP is d,l-N-[4-[1-hydroxy-2-[(1-methylethyl) amino]ethyl]phenyl]methane-sulfonamide monohydrochloride. The molecular formula is C12H20N2O3 S∙HCl and is represented by the following structural formula. SORINE Tablets contain the following inactive ingredients: microcrystalline cellulose, lactose monohydrate, corn starch, stearic acid, magnesium stearate and silicon dioxide."
},
{
"NDCCode": "0268-0012-10",
"PackageDescription": "10 mL in 1 VIAL, MULTI-DOSE (0268-0012-10)",
"NDC11Code": "00268-0012-10",
"ProductNDC": "0268-0012",
"ProductTypeName": "NON-STANDARDIZED ALLERGENIC",
"ProprietaryName": "House Dust",
"NonProprietaryName": "House Dust",
"DosageFormName": "INJECTION, SOLUTION",
"RouteName": "SUBCUTANEOUS",
"StartMarketingDate": "19650101",
"MarketingCategoryName": "BLA",
"ApplicationNumber": "BLA103753",
"LabelerName": "ALK-Abello, Inc.",
"SubstanceName": "HOUSE DUST",
"StrengthNumber": ".1",
"StrengthUnit": "g/mL",
"Pharm_Classes": "Non-Standardized House Dust Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],House Dust [Chemical/Ingredient]",
"Status": "Deprecated",
"LastUpdate": "2016-12-02"
},
{
"NDCCode": "0268-0012-50",
"PackageDescription": "50 mL in 1 VIAL, MULTI-DOSE (0268-0012-50)",
"NDC11Code": "00268-0012-50",
"ProductNDC": "0268-0012",
"ProductTypeName": "NON-STANDARDIZED ALLERGENIC",
"ProprietaryName": "House Dust",
"NonProprietaryName": "House Dust",
"DosageFormName": "INJECTION, SOLUTION",
"RouteName": "SUBCUTANEOUS",
"StartMarketingDate": "19650101",
"MarketingCategoryName": "BLA",
"ApplicationNumber": "BLA103753",
"LabelerName": "ALK-Abello, Inc.",
"SubstanceName": "HOUSE DUST",
"StrengthNumber": ".1",
"StrengthUnit": "g/mL",
"Pharm_Classes": "Non-Standardized House Dust Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],House Dust [Chemical/Ingredient]",
"Status": "Deprecated",
"LastUpdate": "2016-12-02"
},
{
"NDCCode": "0327-0012-30",
"PackageDescription": "30 BOTTLE in 1 CARTON (0327-0012-30) > 30 mL in 1 BOTTLE",
"NDC11Code": "00327-0012-30",
"ProductNDC": "0327-0012",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Renacidin",
"NonProprietaryName": "Citric Acid, Gluconolactone And Magnesium Carbonate",
"DosageFormName": "SOLUTION",
"RouteName": "IRRIGATION",
"StartMarketingDate": "20160201",
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA019481",
"LabelerName": "United-Guardian, Inc.",
"SubstanceName": "ANHYDROUS CITRIC ACID; GLUCONOLACTONE; MAGNESIUM CARBONATE",
"StrengthNumber": "6.602; .198; 3.268",
"StrengthUnit": "g/100mL; g/100mL; g/100mL",
"Pharm_Classes": "Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Irrigation [MoA]",
"Status": "Active",
"LastUpdate": "2020-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20160201",
"SamplePackage": "N",
"IndicationAndUsage": "Renacidin is indicated for dissolution of bladder calculi of the struvite or apatite variety by local intermittent irrigation through a urethral catheter or cystostomy tube as an alternative or adjunct to surgical procedures. Renacidin is also indicated for use as an intermittent irrigating solution to prevent encrustations of indwelling urethral catheters and cystostomy tubes.",
"Description": "Renacidin® (Citric Acid, Glucono delta-lactone, and Magnesium Carbonate) is a sterile, non-pyrogenic irrigation solution for use within the lower urinary tract in the dissolution of bladder calculi of the struvite or apatite variety, and prevention of encrustations of urethral catheters and cystostomy tubes. Each 30 mL of Renacidin contains:. Active ingredients: Citric Acid (anhydrous), USP 1980.6 mg C6H8O7Glucono delta-lactone, USP 59.4 mg C6H10O6Magnesium Carbonate, USP 980.4 mg (MgCO3)4 · Mg(OH)2 · 5H2O. Citric Acid. Glucono delta-lactone. Magnesium Carbonate. (MgCO3)4 · Mg(OH)2 · 5H2O. Inert ingredients:Benzoic Acid, USP 6.9 mg Solution pH: 3.85 (3.5-4.2)."
},
{
"NDCCode": "0363-0012-90",
"PackageDescription": "90 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0363-0012-90)",
"NDC11Code": "00363-0012-90",
"ProductNDC": "0363-0012",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Flavor Chews",
"NonProprietaryName": "Calcium Carbonate",
"DosageFormName": "TABLET, CHEWABLE",
"RouteName": "ORAL",
"StartMarketingDate": "20150316",
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part331",
"LabelerName": "Walgreens",
"SubstanceName": "CALCIUM CARBONATE",
"StrengthNumber": "750",
"StrengthUnit": "mg/1",
"Status": "Deprecated",
"LastUpdate": "2018-11-10",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20181231"
}
]
}
{"NDC":[{"NDCCode":"62902-0012-1","ProprietaryName":"Hormone Harmony","NonProprietaryName":"Salsolinol (hydrochloride), Dhea (dehydroepiandrosterone), 7-oxo- Dehydroepiandrosterone-3b-acetate (7-keto), Cholesterinum, Folliculinum, Oophorinum (suis), Progesterone, Testosterone, Cortisone Aceticum, Aldosterone, Androsterone, Follicle Stimulating Hormone"},{"NDCCode":"62902-0001-1","ProprietaryName":"Lean Love","NonProprietaryName":"Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Brain (suis), Hepar Suis, Methylcobalamin, Pancreas Suis, Kidney (suis), Stomach (suis), Aacg-a, Aacg-b, Calcarea Carbonica, Gambogia Gelsemium, Sempervirens Graphites, Nux Vomica, Phytolacca Decandra, 7-keto-dhea (dehydroepiandrosterone), Atp (adenosinum Triphosphoricum Dinatrum), Glucagon, Insulinum, Sarcolacticum Acidum, Proteus (vulgaris)"},{"NDCCode":"62902-0002-1","ProprietaryName":"Craving And Appetite Ease","NonProprietaryName":"Acetyl Coenzyme A, Adenosinum Triphosphoricum Dinatrum, Adrenal Cortex (suis), Bacopa Speciosa, Dopamine Hydrochloride, Equol, Gambogia, Oxytocin Acetate, Rhodiola, Stomach (suis), Thyroidinum (suis), Chininum Sulphuricum, Cina, Iodium, Lycopodium Clavatum, Phosphorus, Serotonin (hydrochloride), Morgan Gaertner"},{"NDCCode":"62902-0003-1","ProprietaryName":"Metabolic Rewire Support","NonProprietaryName":"Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Hepar Suis, Kidney (suis), Methylcobalamin, Gambogia, Graphites, Nux Vomica, Phytolacca Decandra, 7-keto (3-acetyl-7-oxo-dehydroepiandrosterone), Adenosinum Triphosphoricum Dinatrum, Glucagon, Insulinum (suis), Sarcolacticum Acidum, Proteus (vulgaris)"},{"NDCCode":"62902-0004-1","ProprietaryName":"Hgh Vibrancy","NonProprietaryName":"Agnus Castus, Ambra Grisea, Conium Maculatum, Apiolum, Estradiol, Estriol, Folliculinum, L-dopa, Melatonin, Testosterone, Alpha-lipoicum Acidum, Adenosinum Triphosphoricum Dinatrum, Coenzyme A, Ubidecarenonum, Nadidum, Sarcolacticum Acidum, Baryta Carbonica, Selenium Metallicum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (suis), Lymph Node(suis), Medulla Ossis Suis, Oophorinum (suis), Orchitinum (suis), Pancreas Suis, Spleen (suis)"},{"NDCCode":"62902-0005-1","ProprietaryName":"Clean Sweep Formula 1","NonProprietaryName":"Acetylcholine Chloride, Adrenalinum, Dopamine Hydrochloride, Gaba, Norepinephrine, Octopamine (hydrochloride), Serotonin (hydrochloride), Taurine, Adenosinum Cyclophosphoricum, Cerebrum (suis), Diencephalon (suis), Pineal Gland (suis), Thalamus Opticus,"},{"NDCCode":"62902-0006-1","ProprietaryName":"Clean Sweep Formula 2","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, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Gnaphalium Polycephalum"},{"NDCCode":"62902-0007-1","ProprietaryName":"Clean Sweep Formula 3","NonProprietaryName":"Ceanothus Americanus, Veratrum Album, Anacardium Orientale, Argentum Nitricum, Condurango, Hydrastis Canadensis, Momordica Balsamina, Oxalis Acetosella, Pulsatilla (vulgaris), 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, Rectal Mucosa (suis), Stomach (suis)"},{"NDCCode":"62902-0008-1","ProprietaryName":"Clean Sweep Formula 4","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, Alpha-ketoglutaricum Acidum, Cholesterinum, Formicum Acidum, Glyoxal Trimer Dihydrate, Histaminum Hydrochloricum, Malicum Acidum, Natrum Oxalaceticum, Sulphur, Calcarea Carbonica"},{"NDCCode":"62902-0009-1","ProprietaryName":"Clean Sweep Formula 5","NonProprietaryName":"Solidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, Equisetum Hyemale, Argentum Nitricum, Cantharis, Capsicum Annuum, Cuprum Sulphuricum, Orthosiphon Stamineus, Pareira Brava, Sarsaparilla (smilax Regelii), Terebinthina, Apis Venenum Purum, Barosma (betulina), 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"},{"NDCCode":"62902-0010-1","ProprietaryName":"Clean Sweep Formula 6","NonProprietaryName":"Conium Maculatum, Dulcamara, Echinacea (angustifolia), Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbic Acid, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Pulsatilla (vulgaris), Sarcolacticum Acidum, Lymph Node (suis), Sulphur, Glandula Suprarenalis Suis, L-phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus (suis), Spleen (suis), Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Glyphosate, Funiculus Umbilicalis Suis"},{"NDCCode":"62902-0011-1","ProprietaryName":"Lean Love","NonProprietaryName":"Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Cerebrum Suis, Hepar Suis, Methylcobalamin, Pancreas Suis, Kidney (suis), Stomach (suis), Aacg-a, Aacg-b, Calcarea Carbonica, Gambogia Gelsemium, Sempervirens Graphites, Nux Vomica, Phytolacca Decandra, 7-keto (3-acetyl-7-oxo-dehyroepiandrosterone), Adenosinum Triphosphoricum Dinatrum, Glucagon, Insulinum (suis), Sarcolacticum Acidum, Proteus (vulgaris)"},{"NDCCode":"62902-0013-1","ProprietaryName":"Hgh Vibrancy","NonProprietaryName":"Agnus Castus, Ambra Grisea, Conium Maculatum, Apiolum, Estradiol, Estriol, Folliculinum, L-dopa, Melatonin, Testosterone, Alpha-lipoicum Acidum, Adenosinum Triphosphoricum Dinatrum, Ubidecarenonum, Nadidum, Sarcolacticum Acidum, Baryta Carbonica, Selenium Metallicum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (suis), Lymph Node(suis), Medulla Ossis Suis, Oophorinum (suis), Orchitinum (suis), Pancreas Suis, Spleen (suis), Human Growth Hormone, Proteus (morgani)"},{"NDCCode":"0009-0012-01","ProprietaryName":"Cortef","NonProprietaryName":"Hydrocortisone"},{"NDCCode":"0054-0012-20","ProprietaryName":"Flecainide Acetate","NonProprietaryName":"Flecainide Acetate"},{"NDCCode":"0054-0012-21","ProprietaryName":"Flecainide Acetate","NonProprietaryName":"Flecainide Acetate"},{"NDCCode":"0054-0012-25","ProprietaryName":"Flecainide Acetate","NonProprietaryName":"Flecainide Acetate"},{"NDCCode":"0093-0012-98","ProprietaryName":"Pantoprazole Sodium","NonProprietaryName":"Pantoprazole Sodium"},{"NDCCode":"0168-0012-09","ProprietaryName":"Triple Antibiotic","NonProprietaryName":"Neomycin And Polymyxin B Sulfates And Bacitracin Zinc"},{"NDCCode":"0168-0012-31","ProprietaryName":"Triple Antibiotic","NonProprietaryName":"Neomycin And Polymyxin B Sulfates And Bacitracin Zinc"},{"NDCCode":"0168-0012-35","ProprietaryName":"Triple Antibiotic","NonProprietaryName":"Neomycin And Polymyxin B Sulfates And Bacitracin Zinc"},{"NDCCode":"0187-0011-10","ProprietaryName":"Iprivask","NonProprietaryName":"Desirudin"},{"NDCCode":"0220-0012-11","NonProprietaryName":"Artemisia Abrotanum Flowering Top"},{"NDCCode":"0220-0012-12","NonProprietaryName":"Artemisia Abrotanum Flowering Top"},{"NDCCode":"0245-0012-01","ProprietaryName":"Sorine","NonProprietaryName":"Sotalol Hydrochloride"},{"NDCCode":"0245-0012-11","ProprietaryName":"Sorine","NonProprietaryName":"Sotalol Hydrochloride"},{"NDCCode":"0268-0012-10","ProprietaryName":"House Dust","NonProprietaryName":"House Dust"},{"NDCCode":"0268-0012-50","ProprietaryName":"House Dust","NonProprietaryName":"House Dust"},{"NDCCode":"0327-0012-30","ProprietaryName":"Renacidin","NonProprietaryName":"Citric Acid, Gluconolactone And Magnesium Carbonate"},{"NDCCode":"0363-0012-90","ProprietaryName":"Flavor Chews","NonProprietaryName":"Calcium Carbonate"}]}
<?xml version="1.0" encoding="utf-8"?>
<NDCList>
<NDC>
<NDCCode>62902-0012-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0012-1) </PackageDescription>
<NDC11Code>62902-0012-01</NDC11Code>
<ProductNDC>62902-0012</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Hormone Harmony</ProprietaryName>
<NonProprietaryName>Salsolinol (hydrochloride), Dhea (dehydroepiandrosterone), 7-oxo- Dehydroepiandrosterone-3b-acetate (7-keto), Cholesterinum, Folliculinum, Oophorinum (suis), Progesterone, Testosterone, Cortisone Aceticum, Aldosterone, Androsterone, Follicle Stimulating Hormone</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20181022</StartMarketingDate>
<EndMarketingDate>20231212</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>7-OXODEHYDROEPIANDROSTERONE 3-ACETATE; ALDOSTERONE; ANDROSTERONE; CHOLESTEROL; CORTISONE ACETATE; ESTRONE; FOLLITROPIN; PRASTERONE; PROGESTERONE; SALSOLINOL HYDROCHLORIDE, (+/-)-; SUS SCROFA OVARY; TESTOSTERONE</SubstanceName>
<StrengthNumber>8; 12; 12; 8; 12; 8; 12; 6; 8; 6; 8; 8</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Gonadotropin [EPC], Gonadotropins [CS], Progesterone [CS], Progesterone [EPC]</Pharm_Classes>
<DEASchedule>CIII</DEASchedule>
<Status>Deprecated</Status>
<LastUpdate>2023-12-13</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20181022</StartMarketingDatePackage>
<EndMarketingDatePackage>20231212</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>62902-0001-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0001-1)</PackageDescription>
<NDC11Code>62902-0001-01</NDC11Code>
<ProductNDC>62902-0001</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Lean Love</ProprietaryName>
<NonProprietaryName>Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Brain (suis), Hepar Suis, Methylcobalamin, Pancreas Suis, Kidney (suis), Stomach (suis), Aacg-a, Aacg-b, Calcarea Carbonica, Gambogia Gelsemium, Sempervirens Graphites, Nux Vomica, Phytolacca Decandra, 7-keto-dhea (dehydroepiandrosterone), Atp (adenosinum Triphosphoricum Dinatrum), Glucagon, Insulinum, Sarcolacticum Acidum, Proteus (vulgaris)</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20140522</StartMarketingDate>
<EndMarketingDate>20190513</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>CYNANCHUM VINCETOXICUM ROOT; ECHINACEA ANGUSTIFOLIA; SUS SCROFA HYPOTHALAMUS; PORK BRAIN; PORK LIVER; METHYLCOBALAMIN; SUS SCROFA PANCREAS; PORK KIDNEY; SUS SCROFA STOMACH; APC-356433; APC-356434; OYSTER SHELL CALCIUM CARBONATE, CRUDE; GAMBOGE; GELSEMIUM SEMPERVIRENS ROOT; GRAPHITE; STRYCHNOS NUX-VOMICA SEED; PHYTOLACCA AMERICANA ROOT; 7-KETO-DEHYDROEPIANDROSTERONE; ADENOSINE TRIPHOSPHATE DISODIUM; GLUCAGON; INSULIN HUMAN; LACTIC ACID, L-; PROTEUS VULGARIS</SubstanceName>
<StrengthNumber>6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 12; 12; 12; 12; 12; 12; 30; 30; 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_C]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2019-05-14</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
</NDC>
<NDC>
<NDCCode>62902-0002-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0002-1) </PackageDescription>
<NDC11Code>62902-0002-01</NDC11Code>
<ProductNDC>62902-0002</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Craving And Appetite Ease</ProprietaryName>
<NonProprietaryName>Acetyl Coenzyme A, Adenosinum Triphosphoricum Dinatrum, Adrenal Cortex (suis), Bacopa Speciosa, Dopamine Hydrochloride, Equol, Gambogia, Oxytocin Acetate, Rhodiola, Stomach (suis), Thyroidinum (suis), Chininum Sulphuricum, Cina, Iodium, Lycopodium Clavatum, Phosphorus, Serotonin (hydrochloride), Morgan Gaertner</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20160824</StartMarketingDate>
<EndMarketingDate>20220602</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>ACETYL COENZYME A; ADENOSINE TRIPHOSPHATE DISODIUM; ARTEMISIA CINA PRE-FLOWERING TOP; BACOPA MONNIERI WHOLE; DOPAMINE HYDROCHLORIDE; EQUOL, (+/-)-; GAMBOGE; IODINE; LYCOPODIUM CLAVATUM SPORE; OXYTOCIN ACETATE; PHOSPHORUS; QUININE SULFATE; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; SEDUM ROSEUM WHOLE; SEROTONIN HYDROCHLORIDE; SUS SCROFA ADRENAL CORTEX; SUS SCROFA STOMACH; SUS SCROFA THYROID</SubstanceName>
<StrengthNumber>6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 30; 6; 6; 6; 6; 6</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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Antimalarial [EPC], Catecholamine [EPC], Catecholamines [CS], Increased Uterine Smooth Muscle Contraction or Tone [PE], Oxytocic [EPC], Oxytocin [CS]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2022-06-03</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20160824</StartMarketingDatePackage>
<EndMarketingDatePackage>20220602</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>62902-0003-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0003-1) </PackageDescription>
<NDC11Code>62902-0003-01</NDC11Code>
<ProductNDC>62902-0003</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Metabolic Rewire Support</ProprietaryName>
<NonProprietaryName>Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Hepar Suis, Kidney (suis), Methylcobalamin, Gambogia, Graphites, Nux Vomica, Phytolacca Decandra, 7-keto (3-acetyl-7-oxo-dehydroepiandrosterone), Adenosinum Triphosphoricum Dinatrum, Glucagon, Insulinum (suis), Sarcolacticum Acidum, Proteus (vulgaris)</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20151012</StartMarketingDate>
<EndMarketingDate>20220602</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>7-KETO-DEHYDROEPIANDROSTERONE; ADENOSINE TRIPHOSPHATE DISODIUM; CYNANCHUM VINCETOXICUM ROOT; ECHINACEA ANGUSTIFOLIA; GAMBOGE; GLUCAGON; GRAPHITE; INSULIN PORK; LACTIC ACID, L-; METHYLCOBALAMIN; PHYTOLACCA AMERICANA ROOT; PORK KIDNEY; PORK LIVER; PROTEUS VULGARIS; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA HYPOTHALAMUS</SubstanceName>
<StrengthNumber>30; 30; 6; 6; 12; 30; 12; 30; 30; 8; 12; 8; 8; 30; 12; 6</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_C]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Allergens [CS], Antihypoglycemic Agent [EPC], Cell-mediated Immunity [PE], Decreased GI Motility [PE], Decreased GI Smooth Muscle Tone [PE], Decreased Glycolysis [PE], Gastrointestinal Motility Inhibitor [EPC], Increased Gluconeogenesis [PE], Increased Glycogenolysis [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2022-06-03</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20151012</StartMarketingDatePackage>
<EndMarketingDatePackage>20220602</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>62902-0004-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0004-1) </PackageDescription>
<NDC11Code>62902-0004-01</NDC11Code>
<ProductNDC>62902-0004</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Hgh Vibrancy</ProprietaryName>
<NonProprietaryName>Agnus Castus, Ambra Grisea, Conium Maculatum, Apiolum, Estradiol, Estriol, Folliculinum, L-dopa, Melatonin, Testosterone, Alpha-lipoicum Acidum, Adenosinum Triphosphoricum Dinatrum, Coenzyme A, Ubidecarenonum, Nadidum, Sarcolacticum Acidum, Baryta Carbonica, Selenium Metallicum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (suis), Lymph Node(suis), Medulla Ossis Suis, Oophorinum (suis), Orchitinum (suis), Pancreas Suis, Spleen (suis)</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20151012</StartMarketingDate>
<EndMarketingDate>20201026</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>CHASTE TREE; AMBERGRIS; CONIUM MACULATUM FLOWERING TOP; APIOLE (PARSLEY); ESTRADIOL; ESTRIOL; ESTRONE; LEVODOPA; MELATONIN; TESTOSTERONE; ADENOSINE TRIPHOSPHATE DISODIUM; .ALPHA.-LIPOIC ACID; COENZYME A; NADIDE; LACTIC ACID, L-; UBIDECARENONE; BARIUM CARBONATE; SELENIUM; SUS SCROFA UMBILICAL CORD; SUS SCROFA ADRENAL GLAND; PORK LIVER; SUS SCROFA HYPOTHALAMUS; SUS SCROFA LYMPH; SUS SCROFA BONE MARROW; SUS SCROFA OVARY; SUS SCROFA TESTICLE; SUS SCROFA PANCREAS; SUS SCROFA SPLEEN; SOMATROPIN; PROTEUS MORGANII</SubstanceName>
<StrengthNumber>6; 6; 6; 6; 6; 6; 6; 6; 6; 6; 8; 8; 8; 8; 8; 8; 8; 8; 30; 30; 30; 30; 30; 30; 30; 30; 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_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2020-10-29</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20151012</StartMarketingDatePackage>
<EndMarketingDatePackage>20201026</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>62902-0005-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0005-1) </PackageDescription>
<NDC11Code>62902-0005-01</NDC11Code>
<ProductNDC>62902-0005</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Clean Sweep Formula 1</ProprietaryName>
<NonProprietaryName>Acetylcholine Chloride, Adrenalinum, Dopamine Hydrochloride, Gaba, Norepinephrine, Octopamine (hydrochloride), Serotonin (hydrochloride), Taurine, Adenosinum Cyclophosphoricum, Cerebrum (suis), Diencephalon (suis), Pineal Gland (suis), Thalamus Opticus,</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20170509</StartMarketingDate>
<EndMarketingDate>20220602</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>.GAMMA.-AMINOBUTYRIC ACID; ACETYLCHOLINE CHLORIDE; ADENOSINE CYCLIC PHOSPHATE; DOPAMINE HYDROCHLORIDE; EPINEPHRINE; NOREPINEPHRINE; OCTOPAMINE HYDROCHLORIDE; SEROTONIN HYDROCHLORIDE; SUS SCROFA CEREBRUM; SUS SCROFA DIENCEPHALON; SUS SCROFA PINEAL GLAND; SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS; TAURINE</SubstanceName>
<StrengthNumber>6; 6; 8; 6; 6; 6; 6; 6; 8; 8; 8; 8; 6</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</StrengthUnit>
<Pharm_Classes>Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Catecholamine [EPC], Catecholamine [EPC], Catecholamine [EPC], Catecholamines [CS], Catecholamines [CS], Catecholamines [CS], Cholinergic Agonists [MoA], Cholinergic Receptor Agonist [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2022-06-03</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20170509</StartMarketingDatePackage>
<EndMarketingDatePackage>20220602</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>62902-0006-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0006-1) </PackageDescription>
<NDC11Code>62902-0006-01</NDC11Code>
<ProductNDC>62902-0006</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Clean Sweep Formula 2</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, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Gnaphalium Polycephalum</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20170510</StartMarketingDate>
<EndMarketingDate>20220602</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>AMMONIUM CHLORIDE; BERBERIS VULGARIS ROOT BARK; BLACK COHOSH; CINCHONA OFFICINALIS BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; CUPRIC ACETATE; ENTEROBACTER CLOACAE; HORSE CHESTNUT; MERCURIC OXIDE; NADIDE; NIACINAMIDE; PANTOTHENIC ACID; PICRIC ACID; PROTEUS MORGANII; PROTEUS VULGARIS; PSEUDOGNAPHALIUM OBTUSIFOLIUM; PYRIDOXINE HYDROCHLORIDE; RANUNCULUS BULBOSUS; RHODODENDRON TOMENTOSUM LEAFY TWIG; RIBOFLAVIN; SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS; SILICON DIOXIDE; SILVER; SODIUM DIETHYL OXALACETATE; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA BONE MARROW; SUS SCROFA CARTILAGE; SUS SCROFA INTERVERTEBRAL DISC; SUS SCROFA UMBILICAL CORD; THIAMINE HYDROCHLORIDE; THIOCTIC ACID; TRIBASIC CALCIUM PHOSPHATE</SubstanceName>
<StrengthNumber>8; 4; 4; 4; 4; 6; 30; 6; 10; 6; 6; 10; 6; 30; 30; 10; 6; 4; 4; 6; 30; 8; 10; 6; 28; 10; 10; 8; 8; 10; 6; 8; 10</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/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_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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>Analogs/Derivatives [Chemical/Ingredient], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2022-06-03</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20170510</StartMarketingDatePackage>
<EndMarketingDatePackage>20220602</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>62902-0007-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0007-1) </PackageDescription>
<NDC11Code>62902-0007-01</NDC11Code>
<ProductNDC>62902-0007</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Clean Sweep Formula 3</ProprietaryName>
<NonProprietaryName>Ceanothus Americanus, Veratrum Album, Anacardium Orientale, Argentum Nitricum, Condurango, Hydrastis Canadensis, Momordica Balsamina, Oxalis Acetosella, Pulsatilla (vulgaris), 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, Rectal Mucosa (suis), Stomach (suis)</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20170510</StartMarketingDate>
<EndMarketingDate>20220602</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>ANEMONE PULSATILLA; ATROPA BELLADONNA; CEANOTHUS AMERICANUS LEAF; GOLDENSEAL; IPECAC; LACHESIS MUTA VENOM; MANDRAGORA OFFICINARUM ROOT; MARSDENIA CONDURANGO BARK; MOMORDICA BALSAMINA IMMATURE FRUIT; OXALIS ACETOSELLA LEAF; PHOSPHORUS; PORK INTESTINE; POTASSIUM DICHROMATE; SEMECARPUS ANACARDIUM JUICE; SHIGELLA DYSENTERIAE; SILVER NITRATE; SODIUM DIETHYL OXALACETATE; SULFUR; SUS SCROFA BILE DUCT; SUS SCROFA COLON; SUS SCROFA DUODENUM; SUS SCROFA ESOPHAGUS; SUS SCROFA EYE; SUS SCROFA GALLBLADDER; SUS SCROFA ILEUM; SUS SCROFA JEJUNUM; SUS SCROFA LUNG; SUS SCROFA NASAL MUCOSA; SUS SCROFA ORAL MUCOSA; SUS SCROFA PANCREAS; SUS SCROFA RECTAL MUCOSA; SUS SCROFA STOMACH; SUS SCROFA URINARY BLADDER; VERATRUM ALBUM ROOT; WOOD CREOSOTE; YEAST MANNAN</SubstanceName>
<StrengthNumber>6; 8; 4; 6; 8; 10; 10; 6; 6; 6; 8; 8; 8; 6; 30; 6; 8; 8; 6; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 6; 4; 10; 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_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_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; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2022-06-03</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20170510</StartMarketingDatePackage>
<EndMarketingDatePackage>20220602</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>62902-0008-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0008-1) </PackageDescription>
<NDC11Code>62902-0008-01</NDC11Code>
<ProductNDC>62902-0008</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Clean Sweep Formula 4</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, Alpha-ketoglutaricum Acidum, Cholesterinum, Formicum Acidum, Glyoxal Trimer Dihydrate, Histaminum Hydrochloricum, Malicum Acidum, Natrum Oxalaceticum, Sulphur, Calcarea Carbonica</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20170511</StartMarketingDate>
<EndMarketingDate>20220601</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>AVENA SATIVA FLOWERING TOP; CHELIDONIUM MAJUS; CHOLESTEROL; CINCHONA OFFICINALIS BARK; CYNARA SCOLYMUS LEAF; FORMIC ACID; GLYOXAL TRIMER DIHYDRATE; HISTAMINE DIHYDROCHLORIDE; LYCOPODIUM CLAVATUM SPORE; MALIC ACID; MENADIONE; METHYLCOBALAMIN; MILK THISTLE; OROTIC ACID; OXOGLURIC ACID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PORK INTESTINE; PORK LIVER; PROTEUS MORGANII; SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS; SODIUM DIETHYL OXALACETATE; SULFUR; SUS SCROFA COLON; SUS SCROFA DUODENUM; SUS SCROFA GALLBLADDER; SUS SCROFA LYMPH; SUS SCROFA PANCREAS; SUS SCROFA THYMUS; TARAXACUM OFFICINALE; THIOCTIC ACID; VERATRUM ALBUM ROOT</SubstanceName>
<StrengthNumber>6; 4; 10; 4; 6; 10; 10; 10; 4; 10; 6; 6; 3; 7; 10; 28; 8; 8; 30; 30; 10; 13; 8; 8; 8; 8; 8; 8; 4; 8; 4</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_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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>2022-06-02</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20170511</StartMarketingDatePackage>
<EndMarketingDatePackage>20220601</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>62902-0009-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0009-1) </PackageDescription>
<NDC11Code>62902-0009-01</NDC11Code>
<ProductNDC>62902-0009</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Clean Sweep Formula 5</ProprietaryName>
<NonProprietaryName>Solidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, Equisetum Hyemale, Argentum Nitricum, Cantharis, Capsicum Annuum, Cuprum Sulphuricum, Orthosiphon Stamineus, Pareira Brava, Sarsaparilla (smilax Regelii), Terebinthina, Apis Venenum Purum, Barosma (betulina), 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>20170512</StartMarketingDate>
<EndMarketingDate>20220601</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>AGATHOSMA BETULINA LEAF; APIS MELLIFERA VENOM; BAPTISIA TINCTORIA ROOT; BERBERIS VULGARIS ROOT BARK; CALCIUM SULFIDE; CAPSICUM; CHONDRODENDRON TOMENTOSUM ROOT; CUPRIC SULFATE; EQUISETUM HYEMALE; ESCHERICHIA COLI; GLYOXAL TRIMER DIHYDRATE; LYTTA VESICATORIA; MERCURIC CHLORIDE; QUERCETIN; SHIGELLA DYSENTERIAE; SILVER NITRATE; SMILAX ORNATA ROOT; SODIUM PYRUVATE; SOLIDAGO VIRGAUREA FLOWERING TOP; SUS SCROFA RENAL PELVIS; SUS SCROFA URETER; SUS SCROFA URETHRA; SUS SCROFA URINARY BLADDER; TURPENTINE OIL</SubstanceName>
<StrengthNumber>8; 8; 4; 4; 10; 6; 6; 6; 4; 15; 8; 6; 8; 10; 30; 6; 6; 10; 3; 8; 8; 8; 8; 6</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_C]/mL; [hp_X]/mL; [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], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2022-06-02</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20170512</StartMarketingDatePackage>
<EndMarketingDatePackage>20220601</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>62902-0010-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0010-1) </PackageDescription>
<NDC11Code>62902-0010-01</NDC11Code>
<ProductNDC>62902-0010</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Clean Sweep Formula 6</ProprietaryName>
<NonProprietaryName>Conium Maculatum, Dulcamara, Echinacea (angustifolia), Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbic Acid, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Pulsatilla (vulgaris), Sarcolacticum Acidum, Lymph Node (suis), Sulphur, Glandula Suprarenalis Suis, L-phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus (suis), Spleen (suis), Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Glyphosate, Funiculus Umbilicalis Suis</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20170512</StartMarketingDate>
<EndMarketingDate>20220601</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>ANTIMONY POTASSIUM TARTRATE; ASCORBIC ACID; BARIUM CARBONATE; BISPHENOL A; BROMINE; CHLORINE; CONIUM MACULATUM FLOWERING TOP; CORTISONE ACETATE; ECHINACEA ANGUSTIFOLIA; ESCHERICHIA COLI; FERRUM PHOSPHORICUM; GALIUM APARINE; GENTIANA LUTEA ROOT; GLYPHOSATE; HORSE CHESTNUT; HYDROFLUORIC ACID; IODINE; LACTIC ACID, L-; LIOTHYRONINE; MERCURIUS SOLUBILIS; PHENYLALANINE; PORK LIVER; PROTORTONIA CACTI; PULSATILLA VULGARIS; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS; SOLANUM DULCAMARA TOP; SULFUR; SUS SCROFA ADRENAL GLAND; SUS SCROFA BONE MARROW; SUS SCROFA HYPOTHALAMUS; SUS SCROFA LYMPH; SUS SCROFA SPLEEN; SUS SCROFA TONSIL; SUS SCROFA UMBILICAL CORD; TRIBASIC CALCIUM PHOSPHATE</SubstanceName>
<StrengthNumber>6; 6; 28; 12; 12; 12; 4; 13; 4; 30; 10; 6; 6; 1000; 6; 12; 12; 6; 10; 13; 8; 10; 6; 6; 9; 4; 8; 8; 12; 10; 6; 10; 6; 6; 10</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Increased Coagulation Factor Activity [PE], Triiodothyronine [CS], Vitamin C [EPC], l-Triiodothyronine [EPC]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2022-06-02</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20170512</StartMarketingDatePackage>
<EndMarketingDatePackage>20220601</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>62902-0011-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0011-1) </PackageDescription>
<NDC11Code>62902-0011-01</NDC11Code>
<ProductNDC>62902-0011</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Lean Love</ProprietaryName>
<NonProprietaryName>Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Cerebrum Suis, Hepar Suis, Methylcobalamin, Pancreas Suis, Kidney (suis), Stomach (suis), Aacg-a, Aacg-b, Calcarea Carbonica, Gambogia Gelsemium, Sempervirens Graphites, Nux Vomica, Phytolacca Decandra, 7-keto (3-acetyl-7-oxo-dehyroepiandrosterone), Adenosinum Triphosphoricum Dinatrum, Glucagon, Insulinum (suis), Sarcolacticum Acidum, Proteus (vulgaris)</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20170509</StartMarketingDate>
<EndMarketingDate>20220607</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>7-KETO-DEHYDROEPIANDROSTERONE; ADENOSINE TRIPHOSPHATE DISODIUM; APC-356433; APC-356434; CYNANCHUM VINCETOXICUM ROOT; ECHINACEA ANGUSTIFOLIA; GAMBOGE; GELSEMIUM SEMPERVIRENS ROOT; GLUCAGON; GRAPHITE; INSULIN PORK; LACTIC ACID, L-; METHYLCOBALAMIN; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; PORK KIDNEY; PORK LIVER; PROTEUS VULGARIS; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA CEREBRUM; SUS SCROFA HYPOTHALAMUS; SUS SCROFA PANCREAS; SUS SCROFA STOMACH</SubstanceName>
<StrengthNumber>30; 30; 8; 8; 6; 6; 12; 12; 30; 12; 30; 30; 8; 12; 12; 8; 8; 30; 12; 8; 6; 8; 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_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Allergens [CS], Antihypoglycemic Agent [EPC], Cell-mediated Immunity [PE], Decreased GI Motility [PE], Decreased GI Smooth Muscle Tone [PE], Decreased Glycolysis [PE], Gastrointestinal Motility Inhibitor [EPC], Increased Gluconeogenesis [PE], Increased Glycogenolysis [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2022-06-08</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20170509</StartMarketingDatePackage>
<EndMarketingDatePackage>20220607</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>62902-0013-1</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, DROPPER (62902-0013-1) </PackageDescription>
<NDC11Code>62902-0013-01</NDC11Code>
<ProductNDC>62902-0013</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Hgh Vibrancy</ProprietaryName>
<NonProprietaryName>Agnus Castus, Ambra Grisea, Conium Maculatum, Apiolum, Estradiol, Estriol, Folliculinum, L-dopa, Melatonin, Testosterone, Alpha-lipoicum Acidum, Adenosinum Triphosphoricum Dinatrum, Ubidecarenonum, Nadidum, Sarcolacticum Acidum, Baryta Carbonica, Selenium Metallicum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (suis), Lymph Node(suis), Medulla Ossis Suis, Oophorinum (suis), Orchitinum (suis), Pancreas Suis, Spleen (suis), Human Growth Hormone, Proteus (morgani)</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20181105</StartMarketingDate>
<EndMarketingDate>20240111</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Intentional Nourishment</LabelerName>
<SubstanceName>.ALPHA.-LIPOIC ACID; ADENOSINE TRIPHOSPHATE DISODIUM; AMBERGRIS; APIOLE (PARSLEY); BARIUM CARBONATE; CHASTE TREE; CONIUM MACULATUM FLOWERING TOP; ESTRADIOL; ESTRIOL; ESTRONE; LACTIC ACID, L-; LEVODOPA; MELATONIN; NADIDE; PANTOTHENIC ACID; PORK LIVER; PROTEUS MORGANII; SELENIUM; SOMATROPIN; SUS SCROFA ADRENAL GLAND; SUS SCROFA BONE MARROW; SUS SCROFA HYPOTHALAMUS; SUS SCROFA LYMPH; SUS SCROFA OVARY; SUS SCROFA PANCREAS; SUS SCROFA SPLEEN; SUS SCROFA TESTICLE; SUS SCROFA UMBILICAL CORD; TESTOSTERONE; UBIDECARENONE</SubstanceName>
<StrengthNumber>8; 8; 6; 6; 8; 6; 8; 6; 6; 8; 8; 6; 6; 8; 8; 30; 30; 8; 30; 30; 30; 30; 30; 30; 30; 30; 30; 30; 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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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>Amino Acids, Aromatic [CS], Androgen Receptor Agonists [MoA], Androgen [EPC], Androstanes [CS], Aromatic Amino Acid [EPC], Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Human Growth Hormone [CS], Recombinant Human Growth Hormone [EPC]</Pharm_Classes>
<DEASchedule>CIII</DEASchedule>
<Status>Deprecated</Status>
<LastUpdate>2024-01-12</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20181105</StartMarketingDatePackage>
<EndMarketingDatePackage>20240111</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For the temporary relief of symptoms related to aging including fatigue, minor joint pain and muscle soreness.**. **These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>0009-0012-01</NDCCode>
<PackageDescription>50 TABLET in 1 BOTTLE (0009-0012-01) </PackageDescription>
<NDC11Code>00009-0012-01</NDC11Code>
<ProductNDC>0009-0012</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Cortef</ProprietaryName>
<NonProprietaryName>Hydrocortisone</NonProprietaryName>
<DosageFormName>TABLET</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>19521215</StartMarketingDate>
<MarketingCategoryName>NDA</MarketingCategoryName>
<ApplicationNumber>NDA008697</ApplicationNumber>
<LabelerName>Pharmacia & Upjohn Company LLC</LabelerName>
<SubstanceName>HYDROCORTISONE</SubstanceName>
<StrengthNumber>5</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Pharm_Classes>Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]</Pharm_Classes>
<Status>Active</Status>
<LastUpdate>2025-02-20</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>19521215</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>CORTEF Tablets are indicated in the following conditions.</IndicationAndUsage>
<Description>CORTEF Tablets contain hydrocortisone which is a glucocorticoid. Glucocorticoids are adrenocortical steroids, both naturally occurring and synthetic, which are readily absorbed from the gastrointestinal tract. Hydrocortisone USP is white to practically white, odorless, crystalline powder with a melting point of about 215° C. It is very slightly soluble in water and in ether; sparingly soluble in acetone and in alcohol; slightly soluble in chloroform. The chemical name for hydrocortisone is pregn-4-ene-3,20-dione,11,17,21-trihydroxy-, (11β)-. Its molecular weight is 362.46 and the structural formula is as outlined below. CORTEF Tablets are available for oral administration in three strengths: each tablet contains either 5 mg, 10 mg, or 20 mg of hydrocortisone. Inactive ingredients: calcium stearate, corn starch, lactose, mineral oil, sorbic acid, sucrose.</Description>
</NDC>
<NDC>
<NDCCode>0054-0012-20</NDCCode>
<PackageDescription>100 BLISTER PACK in 1 CARTON (0054-0012-20) / 1 TABLET in 1 BLISTER PACK</PackageDescription>
<NDC11Code>00054-0012-20</NDC11Code>
<ProductNDC>0054-0012</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Flecainide Acetate</ProprietaryName>
<NonProprietaryName>Flecainide Acetate</NonProprietaryName>
<DosageFormName>TABLET</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20030114</StartMarketingDate>
<MarketingCategoryName>ANDA</MarketingCategoryName>
<ApplicationNumber>ANDA076278</ApplicationNumber>
<LabelerName>Hikma Pharmaceuticals USA Inc.</LabelerName>
<SubstanceName>FLECAINIDE ACETATE</SubstanceName>
<StrengthNumber>150</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Pharm_Classes>Antiarrhythmic [EPC]</Pharm_Classes>
<Status>Active</Status>
<LastUpdate>2024-12-06</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20030114</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>In patients without structural heart disease, flecainide acetate is indicated for the prevention of: 1 paroxysmal supraventricular tachycardias (PSVT), including atrioventricular nodal reentrant tachycardia, atrioventricular reentrant tachycardia and other supraventricular tachycardias of unspecified mechanism associated with disabling symptoms, 2 paroxysmal atrial fibrillation/flutter (PAF) associated with disabling symptoms.</IndicationAndUsage>
<Description>Flecainide Acetate Tablets, USP are an antiarrhythmic drug containing 50 mg, 100 mg or 150 mg of flecainide acetate, USP for oral administration. Flecainide acetate is N-(2-piperidylmethyl)-2,5-bis(2,2,2-trifluoroethoxy)benzamide monoacetate. The structural formula is given below. : 1 .</Description>
</NDC>
<NDC>
<NDCCode>0054-0012-21</NDCCode>
<PackageDescription>60 TABLET in 1 BOTTLE (0054-0012-21) </PackageDescription>
<NDC11Code>00054-0012-21</NDC11Code>
<ProductNDC>0054-0012</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Flecainide Acetate</ProprietaryName>
<NonProprietaryName>Flecainide Acetate</NonProprietaryName>
<DosageFormName>TABLET</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20030114</StartMarketingDate>
<MarketingCategoryName>ANDA</MarketingCategoryName>
<ApplicationNumber>ANDA076278</ApplicationNumber>
<LabelerName>Hikma Pharmaceuticals USA Inc.</LabelerName>
<SubstanceName>FLECAINIDE ACETATE</SubstanceName>
<StrengthNumber>150</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Pharm_Classes>Antiarrhythmic [EPC]</Pharm_Classes>
<Status>Active</Status>
<LastUpdate>2024-12-06</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20030114</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>In patients without structural heart disease, flecainide acetate is indicated for the prevention of: 1 paroxysmal supraventricular tachycardias (PSVT), including atrioventricular nodal reentrant tachycardia, atrioventricular reentrant tachycardia and other supraventricular tachycardias of unspecified mechanism associated with disabling symptoms, 2 paroxysmal atrial fibrillation/flutter (PAF) associated with disabling symptoms.</IndicationAndUsage>
<Description>Flecainide Acetate Tablets, USP are an antiarrhythmic drug containing 50 mg, 100 mg or 150 mg of flecainide acetate, USP for oral administration. Flecainide acetate is N-(2-piperidylmethyl)-2,5-bis(2,2,2-trifluoroethoxy)benzamide monoacetate. The structural formula is given below. : 1 .</Description>
</NDC>
<NDC>
<NDCCode>0054-0012-25</NDCCode>
<PackageDescription>100 TABLET in 1 BOTTLE (0054-0012-25) </PackageDescription>
<NDC11Code>00054-0012-25</NDC11Code>
<ProductNDC>0054-0012</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Flecainide Acetate</ProprietaryName>
<NonProprietaryName>Flecainide Acetate</NonProprietaryName>
<DosageFormName>TABLET</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20030114</StartMarketingDate>
<MarketingCategoryName>ANDA</MarketingCategoryName>
<ApplicationNumber>ANDA076278</ApplicationNumber>
<LabelerName>Hikma Pharmaceuticals USA Inc.</LabelerName>
<SubstanceName>FLECAINIDE ACETATE</SubstanceName>
<StrengthNumber>150</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Pharm_Classes>Antiarrhythmic [EPC]</Pharm_Classes>
<Status>Active</Status>
<LastUpdate>2024-12-06</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20030114</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>In patients without structural heart disease, flecainide acetate is indicated for the prevention of: 1 paroxysmal supraventricular tachycardias (PSVT), including atrioventricular nodal reentrant tachycardia, atrioventricular reentrant tachycardia and other supraventricular tachycardias of unspecified mechanism associated with disabling symptoms, 2 paroxysmal atrial fibrillation/flutter (PAF) associated with disabling symptoms.</IndicationAndUsage>
<Description>Flecainide Acetate Tablets, USP are an antiarrhythmic drug containing 50 mg, 100 mg or 150 mg of flecainide acetate, USP for oral administration. Flecainide acetate is N-(2-piperidylmethyl)-2,5-bis(2,2,2-trifluoroethoxy)benzamide monoacetate. The structural formula is given below. : 1 .</Description>
</NDC>
<NDC>
<NDCCode>0093-0012-98</NDCCode>
<PackageDescription>90 TABLET, DELAYED RELEASE in 1 BOTTLE (0093-0012-98) </PackageDescription>
<NDC11Code>00093-0012-98</NDC11Code>
<ProductNDC>0093-0012</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Pantoprazole Sodium</ProprietaryName>
<NonProprietaryName>Pantoprazole Sodium</NonProprietaryName>
<DosageFormName>TABLET, DELAYED RELEASE</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20071219</StartMarketingDate>
<EndMarketingDate>20200531</EndMarketingDate>
<MarketingCategoryName>ANDA</MarketingCategoryName>
<ApplicationNumber>ANDA077056</ApplicationNumber>
<LabelerName>Teva Pharmaceuticals USA, Inc.</LabelerName>
<SubstanceName>PANTOPRAZOLE SODIUM</SubstanceName>
<StrengthNumber>40</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Pharm_Classes>Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2020-06-02</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20071219</StartMarketingDatePackage>
<EndMarketingDatePackage>20200531</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>0168-0012-09</NDCCode>
<PackageDescription>144 PACKET in 1 CARTON (0168-0012-09) > .9 g in 1 PACKET</PackageDescription>
<NDC11Code>00168-0012-09</NDC11Code>
<ProductNDC>0168-0012</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Triple Antibiotic</ProprietaryName>
<NonProprietaryName>Neomycin And Polymyxin B Sulfates And Bacitracin Zinc</NonProprietaryName>
<DosageFormName>OINTMENT</DosageFormName>
<RouteName>TOPICAL</RouteName>
<StartMarketingDate>20100106</StartMarketingDate>
<MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
<ApplicationNumber>part333B</ApplicationNumber>
<LabelerName>E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.</LabelerName>
<SubstanceName>BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE</SubstanceName>
<StrengthNumber>400; 3.5; 5000</StrengthNumber>
<StrengthUnit>[USP'U]/g; mg/g; [USP'U]/g</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2019-09-21</LastUpdate>
<ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>0168-0012-31</NDCCode>
<PackageDescription>1 TUBE in 1 CARTON (0168-0012-31) > 28.35 g in 1 TUBE</PackageDescription>
<NDC11Code>00168-0012-31</NDC11Code>
<ProductNDC>0168-0012</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Triple Antibiotic</ProprietaryName>
<NonProprietaryName>Neomycin And Polymyxin B Sulfates And Bacitracin Zinc</NonProprietaryName>
<DosageFormName>OINTMENT</DosageFormName>
<RouteName>TOPICAL</RouteName>
<StartMarketingDate>20100106</StartMarketingDate>
<MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
<ApplicationNumber>part333B</ApplicationNumber>
<LabelerName>E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.</LabelerName>
<SubstanceName>BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE</SubstanceName>
<StrengthNumber>400; 3.5; 5000</StrengthNumber>
<StrengthUnit>[USP'U]/g; mg/g; [USP'U]/g</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2019-09-21</LastUpdate>
<ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>0168-0012-35</NDCCode>
<PackageDescription>1 TUBE in 1 CARTON (0168-0012-35) > 14.17 g in 1 TUBE</PackageDescription>
<NDC11Code>00168-0012-35</NDC11Code>
<ProductNDC>0168-0012</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Triple Antibiotic</ProprietaryName>
<NonProprietaryName>Neomycin And Polymyxin B Sulfates And Bacitracin Zinc</NonProprietaryName>
<DosageFormName>OINTMENT</DosageFormName>
<RouteName>TOPICAL</RouteName>
<StartMarketingDate>20100106</StartMarketingDate>
<MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
<ApplicationNumber>part333B</ApplicationNumber>
<LabelerName>E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.</LabelerName>
<SubstanceName>BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE</SubstanceName>
<StrengthNumber>400; 3.5; 5000</StrengthNumber>
<StrengthUnit>[USP'U]/g; mg/g; [USP'U]/g</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2019-09-21</LastUpdate>
<ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>0187-0011-10</NDCCode>
<PackageDescription>1 KIT in 1 PACKAGE (0187-0011-10) * 10 TRAY in 1 PACKAGE > 1 VIAL, SINGLE-DOSE in 1 TRAY > .5 mL in 1 VIAL, SINGLE-DOSE * .6 mL in 1 SYRINGE (0187-0012-01) </PackageDescription>
<NDC11Code>00187-0011-10</NDC11Code>
<ProductNDC>0187-0011</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Iprivask</ProprietaryName>
<NonProprietaryName>Desirudin</NonProprietaryName>
<DosageFormName>KIT</DosageFormName>
<StartMarketingDate>20131231</StartMarketingDate>
<MarketingCategoryName>NDA</MarketingCategoryName>
<ApplicationNumber>NDA021271</ApplicationNumber>
<LabelerName>Valeant Pharmaceuticals North America LLC</LabelerName>
<Status>Deprecated</Status>
<LastUpdate>2018-10-04</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20131231</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>0220-0012-11</NDCCode>
<PackageDescription>30 mL in 1 BOTTLE, GLASS (0220-0012-11)</PackageDescription>
<NDC11Code>00220-0012-11</NDC11Code>
<ProductNDC>0220-0012</ProductNDC>
<ProductTypeName>DRUG FOR FURTHER PROCESSING</ProductTypeName>
<NonProprietaryName>Artemisia Abrotanum Flowering Top</NonProprietaryName>
<DosageFormName>PELLET</DosageFormName>
<StartMarketingDate>20170101</StartMarketingDate>
<MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
<LabelerName>Laboratoires Boiron</LabelerName>
<SubstanceName>ARTEMISIA ABROTANUM FLOWERING TOP</SubstanceName>
<StrengthNumber>1</StrengthNumber>
<StrengthUnit>[hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2014-02-04</LastUpdate>
<ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>0220-0012-12</NDCCode>
<PackageDescription>60 mL in 1 BOTTLE, GLASS (0220-0012-12)</PackageDescription>
<NDC11Code>00220-0012-12</NDC11Code>
<ProductNDC>0220-0012</ProductNDC>
<ProductTypeName>DRUG FOR FURTHER PROCESSING</ProductTypeName>
<NonProprietaryName>Artemisia Abrotanum Flowering Top</NonProprietaryName>
<DosageFormName>PELLET</DosageFormName>
<StartMarketingDate>20170101</StartMarketingDate>
<MarketingCategoryName>DRUG FOR FURTHER PROCESSING</MarketingCategoryName>
<LabelerName>Laboratoires Boiron</LabelerName>
<SubstanceName>ARTEMISIA ABROTANUM FLOWERING TOP</SubstanceName>
<StrengthNumber>1</StrengthNumber>
<StrengthUnit>[hp_X]/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2014-02-04</LastUpdate>
<ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>0245-0012-01</NDCCode>
<PackageDescription>100 BLISTER PACK in 1 CARTON (0245-0012-01) / 1 TABLET in 1 BLISTER PACK (0245-0012-89) </PackageDescription>
<NDC11Code>00245-0012-01</NDC11Code>
<ProductNDC>0245-0012</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Sorine</ProprietaryName>
<NonProprietaryName>Sotalol Hydrochloride</NonProprietaryName>
<DosageFormName>TABLET</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20110215</StartMarketingDate>
<EndMarketingDate>20250131</EndMarketingDate>
<MarketingCategoryName>ANDA</MarketingCategoryName>
<ApplicationNumber>ANDA075500</ApplicationNumber>
<LabelerName>Upsher-Smith Laboratories, Inc.</LabelerName>
<SubstanceName>SOTALOL HYDROCHLORIDE</SubstanceName>
<StrengthNumber>80</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Pharm_Classes>Adrenergic beta-Antagonists [MoA], Antiarrhythmic [EPC], Cardiac Rhythm Alteration [PE]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2024-06-01</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20110215</StartMarketingDatePackage>
<EndMarketingDatePackage>20240531</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>SORINE (sotalol hydrochloride) is an antiarrhythmic indicated for: 1 the treatment of life-threatening ventricular arrhythmias (1.1), 2 the maintenance of normal sinus rhythm in patients with atrial fibrillation or flutter (AFIB/AFL) (1.2).</IndicationAndUsage>
<Description>SORINE contains sotalol hydrochloride, USP an antiarrhythmic drug with Class II (beta-adrenoreceptor blocking) and Class III (cardiac action potential duration prolongation) properties. SORINE (sotalol hydrochloride, USP) is supplied as a white, capsule-shaped tablet for oral administration. Sotalol hydrochloride, USP is a white, crystalline solid with a molecular weight of 308.8. It is hydrophilic, soluble in water, propylene glycol and ethanol, but is only slightly soluble in chloroform. Chemically, sotalol hydrochloride, USP is d,l-N-[4-[1-hydroxy-2-[(1-methylethyl) amino]ethyl]phenyl]methane-sulfonamide monohydrochloride. The molecular formula is C12H20N2O3 S∙HCl and is represented by the following structural formula. SORINE Tablets contain the following inactive ingredients: microcrystalline cellulose, lactose monohydrate, corn starch, stearic acid, magnesium stearate and silicon dioxide.</Description>
</NDC>
<NDC>
<NDCCode>0245-0012-11</NDCCode>
<PackageDescription>100 TABLET in 1 BOTTLE (0245-0012-11) </PackageDescription>
<NDC11Code>00245-0012-11</NDC11Code>
<ProductNDC>0245-0012</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Sorine</ProprietaryName>
<NonProprietaryName>Sotalol Hydrochloride</NonProprietaryName>
<DosageFormName>TABLET</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20110215</StartMarketingDate>
<MarketingCategoryName>ANDA</MarketingCategoryName>
<ApplicationNumber>ANDA075500</ApplicationNumber>
<LabelerName>Upsher-Smith Laboratories, Inc.</LabelerName>
<SubstanceName>SOTALOL HYDROCHLORIDE</SubstanceName>
<StrengthNumber>80</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Pharm_Classes>Adrenergic beta-Antagonists [MoA], Antiarrhythmic [EPC], Cardiac Rhythm Alteration [PE]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2024-01-02</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20231231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20110215</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>SORINE (sotalol hydrochloride) is an antiarrhythmic indicated for: 1 the treatment of life-threatening ventricular arrhythmias (1.1), 2 the maintenance of normal sinus rhythm in patients with atrial fibrillation or flutter (AFIB/AFL) (1.2).</IndicationAndUsage>
<Description>SORINE contains sotalol hydrochloride, USP an antiarrhythmic drug with Class II (beta-adrenoreceptor blocking) and Class III (cardiac action potential duration prolongation) properties. SORINE (sotalol hydrochloride, USP) is supplied as a white, capsule-shaped tablet for oral administration. Sotalol hydrochloride, USP is a white, crystalline solid with a molecular weight of 308.8. It is hydrophilic, soluble in water, propylene glycol and ethanol, but is only slightly soluble in chloroform. Chemically, sotalol hydrochloride, USP is d,l-N-[4-[1-hydroxy-2-[(1-methylethyl) amino]ethyl]phenyl]methane-sulfonamide monohydrochloride. The molecular formula is C12H20N2O3 S∙HCl and is represented by the following structural formula. SORINE Tablets contain the following inactive ingredients: microcrystalline cellulose, lactose monohydrate, corn starch, stearic acid, magnesium stearate and silicon dioxide.</Description>
</NDC>
<NDC>
<NDCCode>0268-0012-10</NDCCode>
<PackageDescription>10 mL in 1 VIAL, MULTI-DOSE (0268-0012-10)</PackageDescription>
<NDC11Code>00268-0012-10</NDC11Code>
<ProductNDC>0268-0012</ProductNDC>
<ProductTypeName>NON-STANDARDIZED ALLERGENIC</ProductTypeName>
<ProprietaryName>House Dust</ProprietaryName>
<NonProprietaryName>House Dust</NonProprietaryName>
<DosageFormName>INJECTION, SOLUTION</DosageFormName>
<RouteName>SUBCUTANEOUS</RouteName>
<StartMarketingDate>19650101</StartMarketingDate>
<MarketingCategoryName>BLA</MarketingCategoryName>
<ApplicationNumber>BLA103753</ApplicationNumber>
<LabelerName>ALK-Abello, Inc.</LabelerName>
<SubstanceName>HOUSE DUST</SubstanceName>
<StrengthNumber>.1</StrengthNumber>
<StrengthUnit>g/mL</StrengthUnit>
<Pharm_Classes>Non-Standardized House Dust Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],House Dust [Chemical/Ingredient]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2016-12-02</LastUpdate>
</NDC>
<NDC>
<NDCCode>0268-0012-50</NDCCode>
<PackageDescription>50 mL in 1 VIAL, MULTI-DOSE (0268-0012-50)</PackageDescription>
<NDC11Code>00268-0012-50</NDC11Code>
<ProductNDC>0268-0012</ProductNDC>
<ProductTypeName>NON-STANDARDIZED ALLERGENIC</ProductTypeName>
<ProprietaryName>House Dust</ProprietaryName>
<NonProprietaryName>House Dust</NonProprietaryName>
<DosageFormName>INJECTION, SOLUTION</DosageFormName>
<RouteName>SUBCUTANEOUS</RouteName>
<StartMarketingDate>19650101</StartMarketingDate>
<MarketingCategoryName>BLA</MarketingCategoryName>
<ApplicationNumber>BLA103753</ApplicationNumber>
<LabelerName>ALK-Abello, Inc.</LabelerName>
<SubstanceName>HOUSE DUST</SubstanceName>
<StrengthNumber>.1</StrengthNumber>
<StrengthUnit>g/mL</StrengthUnit>
<Pharm_Classes>Non-Standardized House Dust Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Allergens [Chemical/Ingredient],House Dust [Chemical/Ingredient]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2016-12-02</LastUpdate>
</NDC>
<NDC>
<NDCCode>0327-0012-30</NDCCode>
<PackageDescription>30 BOTTLE in 1 CARTON (0327-0012-30) > 30 mL in 1 BOTTLE</PackageDescription>
<NDC11Code>00327-0012-30</NDC11Code>
<ProductNDC>0327-0012</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Renacidin</ProprietaryName>
<NonProprietaryName>Citric Acid, Gluconolactone And Magnesium Carbonate</NonProprietaryName>
<DosageFormName>SOLUTION</DosageFormName>
<RouteName>IRRIGATION</RouteName>
<StartMarketingDate>20160201</StartMarketingDate>
<MarketingCategoryName>NDA</MarketingCategoryName>
<ApplicationNumber>NDA019481</ApplicationNumber>
<LabelerName>United-Guardian, Inc.</LabelerName>
<SubstanceName>ANHYDROUS CITRIC ACID; GLUCONOLACTONE; MAGNESIUM CARBONATE</SubstanceName>
<StrengthNumber>6.602; .198; 3.268</StrengthNumber>
<StrengthUnit>g/100mL; g/100mL; g/100mL</StrengthUnit>
<Pharm_Classes>Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Irrigation [MoA]</Pharm_Classes>
<Status>Active</Status>
<LastUpdate>2020-01-01</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20160201</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>Renacidin is indicated for dissolution of bladder calculi of the struvite or apatite variety by local intermittent irrigation through a urethral catheter or cystostomy tube as an alternative or adjunct to surgical procedures. Renacidin is also indicated for use as an intermittent irrigating solution to prevent encrustations of indwelling urethral catheters and cystostomy tubes.</IndicationAndUsage>
<Description>Renacidin® (Citric Acid, Glucono delta-lactone, and Magnesium Carbonate) is a sterile, non-pyrogenic irrigation solution for use within the lower urinary tract in the dissolution of bladder calculi of the struvite or apatite variety, and prevention of encrustations of urethral catheters and cystostomy tubes. Each 30 mL of Renacidin contains:. Active ingredients: Citric Acid (anhydrous), USP 1980.6 mg C6H8O7Glucono delta-lactone, USP 59.4 mg C6H10O6Magnesium Carbonate, USP 980.4 mg (MgCO3)4 · Mg(OH)2 · 5H2O. Citric Acid. Glucono delta-lactone. Magnesium Carbonate. (MgCO3)4 · Mg(OH)2 · 5H2O. Inert ingredients:Benzoic Acid, USP 6.9 mg Solution pH: 3.85 (3.5-4.2).</Description>
</NDC>
<NDC>
<NDCCode>0363-0012-90</NDCCode>
<PackageDescription>90 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0363-0012-90)</PackageDescription>
<NDC11Code>00363-0012-90</NDC11Code>
<ProductNDC>0363-0012</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Flavor Chews</ProprietaryName>
<NonProprietaryName>Calcium Carbonate</NonProprietaryName>
<DosageFormName>TABLET, CHEWABLE</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20150316</StartMarketingDate>
<MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
<ApplicationNumber>part331</ApplicationNumber>
<LabelerName>Walgreens</LabelerName>
<SubstanceName>CALCIUM CARBONATE</SubstanceName>
<StrengthNumber>750</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2018-11-10</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
</NDC>
</NDCList>
<NDCList><NDC><NDCCode>62902-0012-1</NDCCode><ProprietaryName>Hormone Harmony</ProprietaryName><NonProprietaryName>Salsolinol (hydrochloride), Dhea (dehydroepiandrosterone), 7-oxo- Dehydroepiandrosterone-3b-acetate (7-keto), Cholesterinum, Folliculinum, Oophorinum (suis), Progesterone, Testosterone, Cortisone Aceticum, Aldosterone, Androsterone, Follicle Stimulating Hormone</NonProprietaryName></NDC><NDC><NDCCode>62902-0001-1</NDCCode><ProprietaryName>Lean Love</ProprietaryName><NonProprietaryName>Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Brain (suis), Hepar Suis, Methylcobalamin, Pancreas Suis, Kidney (suis), Stomach (suis), Aacg-a, Aacg-b, Calcarea Carbonica, Gambogia Gelsemium, Sempervirens Graphites, Nux Vomica, Phytolacca Decandra, 7-keto-dhea (dehydroepiandrosterone), Atp (adenosinum Triphosphoricum Dinatrum), Glucagon, Insulinum, Sarcolacticum Acidum, Proteus (vulgaris)</NonProprietaryName></NDC><NDC><NDCCode>62902-0002-1</NDCCode><ProprietaryName>Craving And Appetite Ease</ProprietaryName><NonProprietaryName>Acetyl Coenzyme A, Adenosinum Triphosphoricum Dinatrum, Adrenal Cortex (suis), Bacopa Speciosa, Dopamine Hydrochloride, Equol, Gambogia, Oxytocin Acetate, Rhodiola, Stomach (suis), Thyroidinum (suis), Chininum Sulphuricum, Cina, Iodium, Lycopodium Clavatum, Phosphorus, Serotonin (hydrochloride), Morgan Gaertner</NonProprietaryName></NDC><NDC><NDCCode>62902-0003-1</NDCCode><ProprietaryName>Metabolic Rewire Support</ProprietaryName><NonProprietaryName>Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Hepar Suis, Kidney (suis), Methylcobalamin, Gambogia, Graphites, Nux Vomica, Phytolacca Decandra, 7-keto (3-acetyl-7-oxo-dehydroepiandrosterone), Adenosinum Triphosphoricum Dinatrum, Glucagon, Insulinum (suis), Sarcolacticum Acidum, Proteus (vulgaris)</NonProprietaryName></NDC><NDC><NDCCode>62902-0004-1</NDCCode><ProprietaryName>Hgh Vibrancy</ProprietaryName><NonProprietaryName>Agnus Castus, Ambra Grisea, Conium Maculatum, Apiolum, Estradiol, Estriol, Folliculinum, L-dopa, Melatonin, Testosterone, Alpha-lipoicum Acidum, Adenosinum Triphosphoricum Dinatrum, Coenzyme A, Ubidecarenonum, Nadidum, Sarcolacticum Acidum, Baryta Carbonica, Selenium Metallicum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (suis), Lymph Node(suis), Medulla Ossis Suis, Oophorinum (suis), Orchitinum (suis), Pancreas Suis, Spleen (suis)</NonProprietaryName></NDC><NDC><NDCCode>62902-0005-1</NDCCode><ProprietaryName>Clean Sweep Formula 1</ProprietaryName><NonProprietaryName>Acetylcholine Chloride, Adrenalinum, Dopamine Hydrochloride, Gaba, Norepinephrine, Octopamine (hydrochloride), Serotonin (hydrochloride), Taurine, Adenosinum Cyclophosphoricum, Cerebrum (suis), Diencephalon (suis), Pineal Gland (suis), Thalamus Opticus,</NonProprietaryName></NDC><NDC><NDCCode>62902-0006-1</NDCCode><ProprietaryName>Clean Sweep Formula 2</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, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Gnaphalium Polycephalum</NonProprietaryName></NDC><NDC><NDCCode>62902-0007-1</NDCCode><ProprietaryName>Clean Sweep Formula 3</ProprietaryName><NonProprietaryName>Ceanothus Americanus, Veratrum Album, Anacardium Orientale, Argentum Nitricum, Condurango, Hydrastis Canadensis, Momordica Balsamina, Oxalis Acetosella, Pulsatilla (vulgaris), 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, Rectal Mucosa (suis), Stomach (suis)</NonProprietaryName></NDC><NDC><NDCCode>62902-0008-1</NDCCode><ProprietaryName>Clean Sweep Formula 4</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, Alpha-ketoglutaricum Acidum, Cholesterinum, Formicum Acidum, Glyoxal Trimer Dihydrate, Histaminum Hydrochloricum, Malicum Acidum, Natrum Oxalaceticum, Sulphur, Calcarea Carbonica</NonProprietaryName></NDC><NDC><NDCCode>62902-0009-1</NDCCode><ProprietaryName>Clean Sweep Formula 5</ProprietaryName><NonProprietaryName>Solidago Virgaurea, Baptisia Tinctoria, Berberis Vulgaris, Equisetum Hyemale, Argentum Nitricum, Cantharis, Capsicum Annuum, Cuprum Sulphuricum, Orthosiphon Stamineus, Pareira Brava, Sarsaparilla (smilax Regelii), Terebinthina, Apis Venenum Purum, Barosma (betulina), 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>62902-0010-1</NDCCode><ProprietaryName>Clean Sweep Formula 6</ProprietaryName><NonProprietaryName>Conium Maculatum, Dulcamara, Echinacea (angustifolia), Aesculus Hippocastanum, Antimonium Tartaricum, Ascorbic Acid, Coccus Cacti, Galium Aparine, Gentiana Lutea, Geranium Robertianum, Pulsatilla (vulgaris), Sarcolacticum Acidum, Lymph Node (suis), Sulphur, Glandula Suprarenalis Suis, L-phenylalanine, Calcarea Phosphorica, Ferrum Phosphoricum, Hepar Suis, Hypothalamus (suis), Spleen (suis), Cortisone Aceticum, Mercurius Solubilis, Baryta Carbonica, Glyphosate, Funiculus Umbilicalis Suis</NonProprietaryName></NDC><NDC><NDCCode>62902-0011-1</NDCCode><ProprietaryName>Lean Love</ProprietaryName><NonProprietaryName>Asclepias Vincetoxicum, Echinacea (angustifolia), Hypothalamus (suis), Cerebrum Suis, Hepar Suis, Methylcobalamin, Pancreas Suis, Kidney (suis), Stomach (suis), Aacg-a, Aacg-b, Calcarea Carbonica, Gambogia Gelsemium, Sempervirens Graphites, Nux Vomica, Phytolacca Decandra, 7-keto (3-acetyl-7-oxo-dehyroepiandrosterone), Adenosinum Triphosphoricum Dinatrum, Glucagon, Insulinum (suis), Sarcolacticum Acidum, Proteus (vulgaris)</NonProprietaryName></NDC><NDC><NDCCode>62902-0013-1</NDCCode><ProprietaryName>Hgh Vibrancy</ProprietaryName><NonProprietaryName>Agnus Castus, Ambra Grisea, Conium Maculatum, Apiolum, Estradiol, Estriol, Folliculinum, L-dopa, Melatonin, Testosterone, Alpha-lipoicum Acidum, Adenosinum Triphosphoricum Dinatrum, Ubidecarenonum, Nadidum, Sarcolacticum Acidum, Baryta Carbonica, Selenium Metallicum, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis, Hepar Suis, Hypothalamus (suis), Lymph Node(suis), Medulla Ossis Suis, Oophorinum (suis), Orchitinum (suis), Pancreas Suis, Spleen (suis), Human Growth Hormone, Proteus (morgani)</NonProprietaryName></NDC><NDC><NDCCode>0009-0012-01</NDCCode><ProprietaryName>Cortef</ProprietaryName><NonProprietaryName>Hydrocortisone</NonProprietaryName></NDC><NDC><NDCCode>0054-0012-20</NDCCode><ProprietaryName>Flecainide Acetate</ProprietaryName><NonProprietaryName>Flecainide Acetate</NonProprietaryName></NDC><NDC><NDCCode>0054-0012-21</NDCCode><ProprietaryName>Flecainide Acetate</ProprietaryName><NonProprietaryName>Flecainide Acetate</NonProprietaryName></NDC><NDC><NDCCode>0054-0012-25</NDCCode><ProprietaryName>Flecainide Acetate</ProprietaryName><NonProprietaryName>Flecainide Acetate</NonProprietaryName></NDC><NDC><NDCCode>0093-0012-98</NDCCode><ProprietaryName>Pantoprazole Sodium</ProprietaryName><NonProprietaryName>Pantoprazole Sodium</NonProprietaryName></NDC><NDC><NDCCode>0168-0012-09</NDCCode><ProprietaryName>Triple Antibiotic</ProprietaryName><NonProprietaryName>Neomycin And Polymyxin B Sulfates And Bacitracin Zinc</NonProprietaryName></NDC><NDC><NDCCode>0168-0012-31</NDCCode><ProprietaryName>Triple Antibiotic</ProprietaryName><NonProprietaryName>Neomycin And Polymyxin B Sulfates And Bacitracin Zinc</NonProprietaryName></NDC><NDC><NDCCode>0168-0012-35</NDCCode><ProprietaryName>Triple Antibiotic</ProprietaryName><NonProprietaryName>Neomycin And Polymyxin B Sulfates And Bacitracin Zinc</NonProprietaryName></NDC><NDC><NDCCode>0187-0011-10</NDCCode><ProprietaryName>Iprivask</ProprietaryName><NonProprietaryName>Desirudin</NonProprietaryName></NDC><NDC><NDCCode>0220-0012-11</NDCCode><NonProprietaryName>Artemisia Abrotanum Flowering Top</NonProprietaryName></NDC><NDC><NDCCode>0220-0012-12</NDCCode><NonProprietaryName>Artemisia Abrotanum Flowering Top</NonProprietaryName></NDC><NDC><NDCCode>0245-0012-01</NDCCode><ProprietaryName>Sorine</ProprietaryName><NonProprietaryName>Sotalol Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>0245-0012-11</NDCCode><ProprietaryName>Sorine</ProprietaryName><NonProprietaryName>Sotalol Hydrochloride</NonProprietaryName></NDC><NDC><NDCCode>0268-0012-10</NDCCode><ProprietaryName>House Dust</ProprietaryName><NonProprietaryName>House Dust</NonProprietaryName></NDC><NDC><NDCCode>0268-0012-50</NDCCode><ProprietaryName>House Dust</ProprietaryName><NonProprietaryName>House Dust</NonProprietaryName></NDC><NDC><NDCCode>0327-0012-30</NDCCode><ProprietaryName>Renacidin</ProprietaryName><NonProprietaryName>Citric Acid, Gluconolactone And Magnesium Carbonate</NonProprietaryName></NDC><NDC><NDCCode>0363-0012-90</NDCCode><ProprietaryName>Flavor Chews</ProprietaryName><NonProprietaryName>Calcium Carbonate</NonProprietaryName></NDC></NDCList>