{
"NDC": [
{
"NDCCode": "55146-006-01",
"PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (55146-006-01) ",
"NDC11Code": "55146-0006-01",
"ProductNDC": "55146-006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "6 Environmental Detox",
"NonProprietaryName": "Baptisia Tinctoria, Phytolacca Decandra, Spigelia Anthelmia, Adrenocorticotrophin, Aluminum Metallicum, Apis Mellifica, Argentum Nitricum, Arsenicum Album, Benzoicum Acidum, Calcarea Carbonica, Carbo Vegetabilis, Kali Phosphoricum, Magnesia Sulphurica, Mercurius Solubilis, Nitricum Acidum, Nux Vomica, Phosphorus, Silicea",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20190611",
"EndMarketingDate": "20251211",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Biotics Research Corporation",
"SubstanceName": "ACTIVATED CHARCOAL; ALUMINUM; APIS MELLIFERA; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BENZOIC ACID; CORTICOTROPIN; MAGNESIUM SULFATE HEPTAHYDRATE; MERCURIUS SOLUBILIS; NITRIC ACID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; POTASSIUM PHOSPHATE, DIBASIC; SILICON DIOXIDE; SILVER NITRATE; SPIGELIA ANTHELMIA WHOLE; STRYCHNOS NUX-VOMICA SEED",
"StrengthNumber": "30; 30; 30; 30; 3; 30; 30; 30; 30; 30; 30; 30; 4; 30; 30; 30; 6; 30",
"StrengthUnit": "[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL",
"Pharm_Classes": "Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Allergens [CS], Ammonium Ion Binding Activity [MoA], Bee Venoms [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Nitrogen Binding Agent [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
"Status": "Deprecated",
"LastUpdate": "2025-12-16",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20190611",
"EndMarketingDatePackage": "20251211",
"SamplePackage": "N",
"IndicationAndUsage": "For temporary relief of cough, rattling in chest, hoarseness, sore throat, skin irritation and vomiting upon environmental exposure. Remedy # 6 supports detoxification of insecticides, environmental and industrial pollutants."
},
{
"NDCCode": "55146-001-01",
"PackageDescription": "120 mL in 1 BOTTLE (55146-001-01) ",
"NDC11Code": "55146-0001-01",
"ProductNDC": "55146-001",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "1 Detoxification",
"NonProprietaryName": "Capsicum Annuum, Phytolacca Decandra, Trifolium Pratense, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium Metallicum, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Oxydatum, Ferrum Metallicum, Gadolinium Oxydatum, Germanium Sesquioxide, Holmium,",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20190610",
"EndMarketingDate": "20250625",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Biotics Research Corporation",
"SubstanceName": "ACTIVATED CHARCOAL; ALCOHOL, X-RAY EXPOSED (1000 RAD); ALLYLTHIOUREA; ALUMINUM; ANGUILLA ROSTRATA BLOOD SERUM; ANTIMONY TRISULFIDE; APIS MELLIFERA; ARSENIC TRIOXIDE; BACILLUS ANTHRACIS IMMUNOSERUM RABBIT; BARIUM CARBONATE; BERYLLIUM; BISMUTH; BORON; BROMINE; CADMIUM; CAPSICUM; CARBO ANIMALIS; CERIUM; CESIUM CHLORIDE; CHROMIUM; CLAVICEPS PURPUREA SCLEROTIUM; COBALT; CONIUM MACULATUM FLOWERING TOP; COPPER; CORTICOTROPIN; DYSPROSIUM; ERBIUM; EUROPIUM; GADOLINIUM; GELSEMIUM SEMPERVIRENS ROOT; GERMANIUM SESQUIOXIDE; GOLD; HOLMIUM; HUMAN BREAST TUMOR CELL; INDIUM; IRON; LACHESIS MUTA VENOM; LANTHANUM; LEAD; LITHIUM CARBONATE; MAGNESIUM; MANGANESE; MERCURIUS SOLUBILIS; MOLYBDENUM; NEODYMIUM OXIDE; NICKEL; NIOBIUM; OSMIUM; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PALLADIUM; PHOSPHORIC ACID; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PLATINUM; POTASSIUM DICHROMATE; PRASEODYMIUM; RANCID BEEF; RHODIUM; RUBIDIUM NITRITE; SAMARIUM; SELENIUM; SILVER; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRONTIUM CARBONATE; STRYCHNOS WALLICHIANA BARK; SULFURIC ACID; SUS SCROFA PITUITARY GLAND; TANTALUM; TARTARIC ACID; TERBIUM; THALLIUM; THERIDION CURASSAVICUM; THUJA OCCIDENTALIS LEAFY TWIG; THYROID; TIN; TRIFOLIUM PRATENSE FLOWER; URANYL NITRATE HEXAHYDRATE; VANADIUM; VERATRUM ALBUM ROOT; YTTERBIUM OXIDE; ZINC",
"StrengthNumber": "30; 30; 30; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 30; 12; 3; 30; 12; 12; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 30; 12; 12; 12; 30; 12; 12; 30; 14; 12; 12; 12; 12; 12; 12; 12; 12; 30; 12; 30; 12; 30; 30; 4; 12; 30; 12; 30; 12; 12; 12; 12; 12; 30; 12; 30; 30; 30; 30; 30; 12; 12; 30; 30; 30; 12; 3; 12; 12; 30; 12; 12",
"StrengthUnit": "[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_X]/mL; [hp_C]/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_C]/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_C]/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_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/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_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/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_C]/mL; [hp_X]/mL; [hp_X]/mL",
"Pharm_Classes": "Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Mood Stabilizer [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS]",
"Status": "Deprecated",
"LastUpdate": "2025-06-26",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20190610",
"EndMarketingDatePackage": "20250625",
"SamplePackage": "N",
"IndicationAndUsage": "For temporary relief of gastrointestinal dyspepsia (indigestion) with flatulence, bloating and intolerance of certain foods. Remedy #1 supports detoxification and cellular repair."
},
{
"NDCCode": "55146-002-01",
"PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (55146-002-01) ",
"NDC11Code": "55146-0002-01",
"ProductNDC": "55146-002",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "2 Lymphatic Drainage",
"NonProprietaryName": "Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, Collinsonia Canadensis, Solidago Virgaurea, Hydrastis Canadensis, Fel Tauri, Apis Mellifica, Baryta Muriatica, Ceanothus Americanus, Chininum Sulphuricum, Conium Maculatum, Iodium, Lachesis Mutus, Mercurius Solubilis, Nux Vomica, Phosphorus, Silicea",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20190611",
"EndMarketingDate": "20250821",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Biotics Research Corporation",
"SubstanceName": "APIS MELLIFERA; BARIUM CHLORIDE DIHYDRATE; BERBERIS VULGARIS ROOT BARK; BOS TAURUS BILE; CEANOTHUS AMERICANUS LEAF; CHELIDONIUM MAJUS; COLLINSONIA CANADENSIS ROOT; CONIUM MACULATUM FLOWERING TOP; GOLDENSEAL; IODINE; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; MILK THISTLE; PHOSPHORUS; QUININE SULFATE; SILICON DIOXIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; STRYCHNOS NUX-VOMICA SEED",
"StrengthNumber": "30; 30; 3; 6; 30; 3; 3; 30; 5; 30; 30; 30; 3; 30; 30; 30; 3; 30",
"StrengthUnit": "[hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL",
"Pharm_Classes": "Allergens [CS], Allergens [CS], Antimalarial [EPC], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC]",
"Status": "Deprecated",
"LastUpdate": "2025-08-22",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20190611",
"EndMarketingDatePackage": "20250821",
"SamplePackage": "N",
"IndicationAndUsage": "For temporary relief of fever, sore throat and acute irritation of the bladder. Remedy #2 supports the clearing of organs allowing for lymphatic drainage and detoxification of any stored toxins that have been released during the cleansing."
},
{
"NDCCode": "55146-003-01",
"PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (55146-003-01) ",
"NDC11Code": "55146-0003-01",
"ProductNDC": "55146-003",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "3 Acute Stress",
"NonProprietaryName": "Arnica Montana, Bellis Perennis, Passiflora Incarnata, Valeriana Officinalis, Arsenicum Album, Apis Mellifica, Carcinosin, Cistus Canadensis, Clematis Erecta, Coffea Cruda, Ignatia Amara, Lachesis Mutus, Magnesia Phosphorica, Natrum Muriaticum, Natrum Sulphuricum, Ornithogalum Umbellatum, Phosphoricum Acidum, Salix Nigra, Staphysagria",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20190611",
"EndMarketingDate": "20250716",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Biotics Research Corporation",
"SubstanceName": "APIS MELLIFERA; ARABICA COFFEE BEAN; ARNICA MONTANA WHOLE; ARSENIC TRIOXIDE; BELLIS PERENNIS WHOLE; CLEMATIS RECTA FLOWERING TOP; DELPHINIUM STAPHISAGRIA SEED; HELIANTHEMUM CANADENSE; HUMAN BREAST TUMOR CELL; LACHESIS MUTA VENOM; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; ORNITHOGALUM UMBELLATUM WHOLE; PASSIFLORA INCARNATA FLOWERING TOP; PHOSPHORIC ACID; SALIX NIGRA BARK; SODIUM CHLORIDE; SODIUM SULFATE; STRYCHNOS IGNATII SEED; VALERIAN",
"StrengthNumber": "30; 30; 3; 6; 3; 30; 30; 30; 30; 30; 30; 30; 3; 30; 30; 30; 30; 30; 3",
"StrengthUnit": "[hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL",
"Pharm_Classes": "Allergens [CS], Allergens [CS], Bee Venoms [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
"Status": "Deprecated",
"LastUpdate": "2025-07-17",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20190611",
"EndMarketingDatePackage": "20250716",
"SamplePackage": "N",
"IndicationAndUsage": "For temporary relief of acute stress due to emotional strain, anxiety, sleeplessness, apprehension or fear."
},
{
"NDCCode": "55146-004-01",
"PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (55146-004-01) ",
"NDC11Code": "55146-0004-01",
"ProductNDC": "55146-004",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "4 Detox-virus",
"NonProprietaryName": "Astragalus Membranaceus, Baptisia Tinctoria, Echinacea (echinacea), Phytolacca Decandra, Hydrastis Canadensis, Apis Mellifica, Aranea Diadema, Belladonna, Eupatorium Perfoliatum, Gelsemium Sempervirens, Lachesis Mutus, Phosphoricum Acidum, Silicea, Thuja Occidentalis, Vaccinium Myrtillus",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20190611",
"EndMarketingDate": "20250625",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Biotics Research Corporation",
"SubstanceName": "APIS MELLIFERA; ARANEUS DIADEMATUS; ARSENIC TRIOXIDE; ASTRAGALUS PROPINQUUS ROOT; ATROPA BELLADONNA; BAPTISIA TINCTORIA; BILBERRY; ECHINACEA ANGUSTIFOLIA WHOLE; EUPATORIUM PERFOLIATUM FLOWERING TOP; GELSEMIUM SEMPERVIRENS ROOT; GOLDENSEAL; LACHESIS MUTA VENOM; PHOSPHORIC ACID; PHYTOLACCA AMERICANA ROOT; RANCID BEEF; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAFY TWIG",
"StrengthNumber": "30; 30; 30; 3; 30; 3; 30; 3; 30; 30; 5; 30; 30; 4; 30; 30; 30",
"StrengthUnit": "[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL",
"Pharm_Classes": "Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]",
"Status": "Deprecated",
"LastUpdate": "2025-06-26",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20190611",
"EndMarketingDatePackage": "20250625",
"SamplePackage": "N",
"IndicationAndUsage": "For temporary relief of skin irritation, dry cough, eczema or fever. Remedy #4 supports detoxification of residual toxins left from a viral infection."
},
{
"NDCCode": "55146-005-01",
"PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (55146-005-01) ",
"NDC11Code": "55146-0005-01",
"ProductNDC": "55146-005",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "5 Chronic Stress",
"NonProprietaryName": "Aralia Quinquefolia, Fucus Vesiculosus, Solidago Virgaurea, Taraxacum Officinale, Trifolium Pratense, Hydrastis Canadensis, Arsenicum Album, Calcarea Carbonica, Carbo Vegetabilis, Ceanothus Americanus, Cyclamen Europaeum, Hepar Sulphuris Calcareum, Natrum Muriaticum, Nux Vomica, Petroleum, Phosphorus",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20190611",
"EndMarketingDate": "20250701",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Biotics Research Corporation",
"SubstanceName": "ACTIVATED CHARCOAL; AMERICAN GINSENG; ARSENIC TRIOXIDE; CEANOTHUS AMERICANUS LEAF; CYCLAMEN PURPURASCENS TUBER; FUCUS VESICULOSUS; GOLDENSEAL; KEROSENE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; SODIUM CHLORIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; STRYCHNOS NUX-VOMICA SEED; TARAXACUM OFFICINALE; TRIFOLIUM PRATENSE FLOWER",
"StrengthNumber": "30; 3; 30; 30; 30; 3; 5; 30; 30; 30; 30; 3; 30; 3; 3",
"StrengthUnit": "[hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL",
"Pharm_Classes": "Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]",
"Status": "Deprecated",
"LastUpdate": "2025-07-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20190611",
"EndMarketingDatePackage": "20250701",
"SamplePackage": "N",
"IndicationAndUsage": "For temporary relief of debility or exhaustion after slight exertion, or exhaustion following dysentery. Remedy #5 supports the easing of chronic stress produced by natural substances called adaptogens."
},
{
"NDCCode": "55146-007-01",
"PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (55146-007-01) ",
"NDC11Code": "55146-0007-01",
"ProductNDC": "55146-007",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "7 Heavy Metal Detox",
"NonProprietaryName": "Allium Sativum, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Metallicum, Ferrum Metallicum, Gadolinium Metallicum, Germanium Sesquioxide, Holmium Metallicum, Indium Metallicum, Lithium Carbonicum, Magnesium Metallicum,",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20190611",
"EndMarketingDate": "20250625",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Biotics Research Corporation",
"SubstanceName": "ALUMINUM; ANTIMONY TRISULFIDE; APIS MELLIFERA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BARIUM CARBONATE; BERBERIS VULGARIS ROOT BARK; BERYLLIUM; BISMUTH; BORON; BROMINE; CADMIUM; CALCIUM SULFIDE; CAUSTICUM; CERIUM; CESIUM CHLORIDE; CHROMIUM; COBALT; CONIUM MACULATUM FLOWERING TOP; COPPER; DYSPROSIUM; ERBIUM; EUROPIUM OXIDE; GADOLINIUM; GARLIC; GERMANIUM SESQUIOXIDE; GOLD; HOLMIUM; HYPERICUM PERFORATUM; INDIUM; IPECAC; IRON; LANTHANUM; LEAD; LITHIUM CARBONATE; MAGNESIUM; MANGANESE; MERCURIUS SOLUBILIS; MOLYBDENUM; NEODYMIUM OXIDE; NICKEL; NIOBIUM; OSMIUM; PALLADIUM; PLATINUM; PRASEODYMIUM; RHODIUM; RUBIDIUM NITRITE; SAMARIUM; SELENIUM; SILVER; STRONTIUM CARBONATE; TANTALUM; TERBIUM; THALLIUM; TIN; URANYL NITRATE HEXAHYDRATE; VANADIUM; VERATRUM ALBUM ROOT; YTTERBIUM OXIDE; ZINC",
"StrengthNumber": "12; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 12; 30; 30; 12; 12; 12; 12; 30; 12; 12; 12; 12; 12; 4; 12; 12; 12; 30; 12; 30; 12; 14; 12; 12; 12; 12; 12; 12; 12; 12; 30; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 30; 12; 12; 12; 12; 12; 30; 12; 12",
"StrengthUnit": "[hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/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_C]/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_C]/mL; [hp_X]/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_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_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",
"Pharm_Classes": "Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Mood Stabilizer [EPC], Non-Standardized Food Allergenic Extract [EPC], Plant Proteins [CS], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC]",
"Status": "Deprecated",
"LastUpdate": "2025-06-26",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20190611",
"EndMarketingDatePackage": "20250625",
"SamplePackage": "N",
"IndicationAndUsage": "Temporary relief of neurological disorders, vomiting, prostration and metallic aftertaste. Remedy #7 supports detoxification of environmental pollutants."
},
{
"NDCCode": "55146-008-01",
"PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (55146-008-01) ",
"NDC11Code": "55146-0008-01",
"ProductNDC": "55146-008",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "8 Fungal Yeast Infection",
"NonProprietaryName": "Astragalus Membranaceus, Berberis Vulgaris, Echinacea (angustifolia), Gentiana Lutea, Phytolacca Decandra, Hydrastis Canadensis, Candida Albicans, Apis Mellifica, Calcarea Carbonica, Lycopodium Clavatum, Mercurius Solubilis, Pulsatilla (vulgaris) Sepia, Thuja Occidentalis",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20190611",
"EndMarketingDate": "20230413",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Biotics Research Corporation",
"SubstanceName": "APIS MELLIFERA; ASTRAGALUS PROPINQUUS ROOT; BERBERIS VULGARIS ROOT BARK; CANDIDA ALBICANS; ECHINACEA ANGUSTIFOLIA; GENTIANA LUTEA ROOT; GOLDENSEAL; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; THUJA OCCIDENTALIS LEAF",
"StrengthNumber": "30; 3; 3; 12; 3; 3; 5; 30; 30; 30; 4; 30; 30; 30",
"StrengthUnit": "[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_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL",
"Pharm_Classes": "Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Standardized Insect Venom Allergenic Extract [EPC]",
"Status": "Deprecated",
"LastUpdate": "2023-04-14",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20190611",
"EndMarketingDatePackage": "20230413",
"SamplePackage": "N"
},
{
"NDCCode": "55146-009-01",
"PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (55146-009-01) ",
"NDC11Code": "55146-0009-01",
"ProductNDC": "55146-009",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "9 Bacterial Detox",
"NonProprietaryName": "Baptisia Tinctoria, Dulcamara, Echinacea (angustifolia), Allium Sativum, Phytolacca Decandra, Apis Mellifica, Arsenicum Album, Belladonna, Chamomilla, Ferrum Phosphoricum, Gelsemium Sempervirens, Lachesis Mutus, Mercurius Solubilis, Pyrogenium",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20190611",
"EndMarketingDate": "20250625",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Biotics Research Corporation",
"SubstanceName": "APIS MELLIFERA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BAPTISIA TINCTORIA ROOT; ECHINACEA ANGUSTIFOLIA WHOLE; FERROSOFERRIC PHOSPHATE; GARLIC; GELSEMIUM SEMPERVIRENS ROOT; LACHESIS MUTA VENOM; MATRICARIA CHAMOMILLA WHOLE; MERCURIUS SOLUBILIS; PHYTOLACCA AMERICANA ROOT; RANCID BEEF; SOLANUM DULCAMARA TOP",
"StrengthNumber": "30; 30; 30; 3; 3; 30; 4; 30; 30; 30; 30; 4; 30; 3",
"StrengthUnit": "[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL",
"Pharm_Classes": "Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Plant Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC]",
"Status": "Deprecated",
"LastUpdate": "2025-06-26",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20190611",
"EndMarketingDatePackage": "20250625",
"SamplePackage": "N",
"IndicationAndUsage": "For temporary relief of fever, sore throat and acute irritation of the bladder. Remedy #9 supports detoxification of toxins that remain after a bacterial infection."
},
{
"NDCCode": "55146-010-01",
"PackageDescription": "120 mL in 1 BOTTLE, PLASTIC (55146-010-01) ",
"NDC11Code": "55146-0010-01",
"ProductNDC": "55146-010",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "10 Parasite Detox",
"NonProprietaryName": "Carduus Marianus, Chelidonium Majus, Cina, Sabadilla, Teucrium Marum, Terebinthina, Thyroidinum (suis), Spigelia Anthelmia, Apis Mellifica, Baryta Carbonica, Calcarea Carbonica, Ferrum Muriaticum, Natrum Muriaticum, Silicea, Sulphur",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20190611",
"EndMarketingDate": "20250625",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Biotics Research Corporation",
"SubstanceName": "APIS MELLIFERA; ARTEMISIA CINA PRE-FLOWERING TOP; BARIUM CARBONATE; CHELIDONIUM MAJUS WHOLE; FERRIC CHLORIDE HEXAHYDRATE; MILK THISTLE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SCHOENOCAULON OFFICINALE SEED; SILICON DIOXIDE; SODIUM CHLORIDE; SPIGELIA ANTHELMIA WHOLE; SULFUR; TEUCRIUM MARUM WHOLE; THYROID; TURPENTINE OIL",
"StrengthNumber": "30; 3; 30; 3; 30; 3; 30; 3; 30; 30; 6; 30; 3; 6; 5",
"StrengthUnit": "[hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/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",
"Pharm_Classes": "Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Iron [CS], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Standardized Insect Venom Allergenic Extract [EPC]",
"Status": "Deprecated",
"LastUpdate": "2025-06-26",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20190611",
"EndMarketingDatePackage": "20250625",
"SamplePackage": "N",
"IndicationAndUsage": "For temporary relief of fever, joint pain, cough, stiffness and gastric upset. Remedy #10 supports detoxification of toxins that remain following a parasitic infection."
},
{
"NDCCode": "55146-011-01",
"PackageDescription": "120 mL in 1 BOTTLE (55146-011-01) ",
"NDC11Code": "55146-0011-01",
"ProductNDC": "55146-011",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "1 Detoxification",
"NonProprietaryName": "Trifolium Pratense, Capsicum Annuum, Phytolacca Decandra, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Oxydatum, Ferrum Metallicum, Gadolinium Metallicum, Germanium Sesquioxide, Holmium Metallicum, Indium Metallicum,",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20200505",
"EndMarketingDate": "20250625",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Biotics Research Corporation",
"SubstanceName": "ACTIVATED CHARCOAL; ALCOHOL, X-RAY EXPOSED (1000 RAD); ALLYLTHIOUREA; ALUMINUM; ANGUILLA ROSTRATA BLOOD SERUM; ANTIMONY TRISULFIDE; APIS MELLIFERA; ARSENIC TRIOXIDE; BACILLUS ANTHRACIS IMMUNOSERUM RABBIT; BARIUM CARBONATE; BERYLLIUM; BISMUTH; BORON; BROMINE; CADMIUM; CAPSICUM; CARBO ANIMALIS; CERIUM; CESIUM CHLORIDE; CHROMIUM; CLAVICEPS PURPUREA SCLEROTIUM; COBALT; CONIUM MACULATUM FLOWERING TOP; COPPER; CORTICOTROPIN; DYSPROSIUM; ERBIUM; EUROPIUM; GADOLINIUM; GELSEMIUM SEMPERVIRENS ROOT; GERMANIUM SESQUIOXIDE; GOLD; HOLMIUM; HUMAN BREAST TUMOR CELL; INDIUM; IRON; LACHESIS MUTA VENOM; LANTHANUM; LEAD; LITHIUM CARBONATE; MAGNESIUM; MANGANESE; MERCURIUS SOLUBILIS; MOLYBDENUM; NEODYMIUM OXIDE; NICKEL; NIOBIUM; OSMIUM; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PALLADIUM; PHOSPHORIC ACID; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PLATINUM; POTASSIUM DICHROMATE; PRASEODYMIUM; RANCID BEEF; RHODIUM; RUBIDIUM NITRITE; SAMARIUM; SELENIUM; SILVER; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRONTIUM CARBONATE; STRYCHNOS WALLICHIANA BARK; SULFURIC ACID; SUS SCROFA PITUITARY GLAND; TANTALUM; TARTARIC ACID; TERBIUM; THALLIUM; THERIDION CURASSAVICUM; THUJA OCCIDENTALIS LEAFY TWIG; THYROID; TIN; TRIFOLIUM PRATENSE FLOWER; URANYL NITRATE HEXAHYDRATE; VANADIUM; VERATRUM ALBUM ROOT; YTTERBIUM OXIDE; ZINC",
"StrengthNumber": "30; 30; 30; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 12; 12; 3; 30; 12; 12; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 30; 12; 12; 12; 30; 12; 12; 30; 14; 12; 12; 12; 12; 12; 12; 12; 12; 30; 12; 30; 12; 30; 30; 4; 12; 30; 12; 30; 12; 12; 12; 12; 12; 30; 12; 30; 30; 30; 30; 30; 12; 12; 30; 30; 30; 12; 3; 12; 12; 30; 12; 12",
"StrengthUnit": "[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_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_C]/mL; [hp_X]/mL; [hp_C]/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_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_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/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_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/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_C]/mL; [hp_X]/mL; [hp_X]/mL",
"Pharm_Classes": "Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Mood Stabilizer [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS]",
"Status": "Deprecated",
"LastUpdate": "2025-06-26",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20200505",
"EndMarketingDatePackage": "20250625",
"SamplePackage": "N",
"IndicationAndUsage": "For temporary relief of gastrointestinal dyspepsia (indigestion) with flatulence, bloating and intolerance of certain foods. Remedy #1 supports detoxification and cellular repair."
},
{
"NDCCode": "10014-006-01",
"PackageDescription": "113 L in 1 CYLINDER (10014-006-01)",
"NDC11Code": "10014-0006-01",
"ProductNDC": "10014-006",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Oxygen Helium Mixture",
"NonProprietaryName": "Oxygen Helium Mixture",
"DosageFormName": "GAS",
"RouteName": "RESPIRATORY (INHALATION)",
"StartMarketingDate": "19721006",
"MarketingCategoryName": "UNAPPROVED MEDICAL GAS",
"LabelerName": "Aero All Gas Company",
"SubstanceName": "OXYGEN; HELIUM",
"StrengthNumber": "200; 800",
"StrengthUnit": "mL/L; mL/L",
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20171231"
},
{
"NDCCode": "10056-006-01",
"PackageDescription": "280 mL in 1 BOTTLE (10056-006-01) ",
"NDC11Code": "10056-0006-01",
"ProductNDC": "10056-006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Satinique Anti Dandruff",
"NonProprietaryName": "Pyrithione Zinc",
"DosageFormName": "CREAM",
"RouteName": "TOPICAL",
"StartMarketingDate": "20170329",
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "M032",
"LabelerName": "Access Business Group LLC",
"SubstanceName": "PYRITHIONE ZINC",
"StrengthNumber": "9.5",
"StrengthUnit": "mg/mL",
"Status": "Active",
"LastUpdate": "2023-10-24",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20170329",
"SamplePackage": "N",
"IndicationAndUsage": "Controls symptoms of dandruff."
},
{
"NDCCode": "10095-006-01",
"PackageDescription": "15 g in 1 PACKAGE (10095-006-01)",
"NDC11Code": "10095-0006-01",
"ProductNDC": "10095-006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Quitacallos",
"NonProprietaryName": "Salicylic Acid",
"DosageFormName": "CREAM",
"RouteName": "TOPICAL",
"StartMarketingDate": "20150505",
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part358F",
"LabelerName": "World Perfumes, Inc",
"SubstanceName": "SALICYLIC ACID",
"StrengthNumber": "17",
"StrengthUnit": "g/100g",
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20171231",
"IndicationAndUsage": "QuitaCallos. Removedor de Callos. Corn & Callus Remover. Salicylic Acid 17%."
},
{
"NDCCode": "10297-006-01",
"PackageDescription": "85 L in 1 CYLINDER (10297-006-01) ",
"NDC11Code": "10297-0006-01",
"ProductNDC": "10297-006",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Helium",
"NonProprietaryName": "Helium",
"DosageFormName": "GAS",
"RouteName": "RESPIRATORY (INHALATION)",
"StartMarketingDate": "20180601",
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA211781",
"LabelerName": "A-OX Welding Supply, LLC",
"SubstanceName": "HELIUM",
"StrengthNumber": "990",
"StrengthUnit": "mL/L",
"Status": "Active",
"LastUpdate": "2025-12-16",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20180601",
"SamplePackage": "N"
},
{
"NDCCode": "10348-006-01",
"PackageDescription": "1 TUBE in 1 CARTON (10348-006-01) > 50 mL in 1 TUBE",
"NDC11Code": "10348-0006-01",
"ProductNDC": "10348-006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Smashbox",
"ProprietaryNameSuffix": "Photo Finish Foundation Primer Spf 20",
"NonProprietaryName": "Avobenzone, Homosalate, And Octisalate",
"DosageFormName": "LIQUID",
"RouteName": "TOPICAL",
"StartMarketingDate": "20120527",
"MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
"ApplicationNumber": "part352",
"LabelerName": "SMASHBOX BEAUTY COSMETICS, INC",
"SubstanceName": "AVOBENZONE; HOMOSALATE; OCTISALATE",
"StrengthNumber": "2; 15; 5",
"StrengthUnit": "mL/100mL; mL/100mL; mL/100mL",
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20181231",
"IndicationAndUsage": "helps prevent sunburn."
},
{
"NDCCode": "10526-006-01",
"PackageDescription": "230 L in 1 DEWAR (10526-006-01) ",
"NDC11Code": "10526-0006-01",
"ProductNDC": "10526-006",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Nitrogen",
"NonProprietaryName": "Nitrogen",
"DosageFormName": "LIQUID",
"RouteName": "RESPIRATORY (INHALATION)",
"StartMarketingDate": "19900101",
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA205766",
"LabelerName": "Haun Welding Supply, Inc.",
"SubstanceName": "NITROGEN",
"StrengthNumber": "990",
"StrengthUnit": "mL/L",
"Status": "Active",
"LastUpdate": "2025-12-30",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "19900101",
"SamplePackage": "N"
},
{
"NDCCode": "10578-006-01",
"PackageDescription": "28 g in 1 JAR (10578-006-01)",
"NDC11Code": "10578-0006-01",
"ProductNDC": "10578-006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Homeopathic Scar",
"NonProprietaryName": "Pot Marigold, Bushmaster Snake, Black Lead, Oil Of Mustard Seed",
"DosageFormName": "CREAM",
"RouteName": "TOPICAL",
"StartMarketingDate": "20120427",
"MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
"LabelerName": "Indiana Botanic Gardens",
"SubstanceName": "CALENDULA OFFICINALIS FLOWER; LACHESIS MUTA VENOM; GRAPHITE; ALLYLTHIOUREA",
"StrengthNumber": "10; 16; 10; 10",
"StrengthUnit": "[hp_X]/28g; [hp_X]/28g; [hp_X]/28g; [hp_X]/28g",
"Status": "Deprecated",
"LastUpdate": "2020-01-01",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231"
},
{
"NDCCode": "10678-006-01",
"PackageDescription": "566 L in 1 CYLINDER (10678-006-01)",
"NDC11Code": "10678-0006-01",
"ProductNDC": "10678-006",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Nitrous Oxide",
"NonProprietaryName": "Nitrous Oxide",
"DosageFormName": "GAS",
"RouteName": "RESPIRATORY (INHALATION)",
"StartMarketingDate": "19470523",
"MarketingCategoryName": "UNAPPROVED MEDICAL GAS",
"LabelerName": "Airgas-West, Inc.",
"SubstanceName": "NITROUS OXIDE",
"StrengthNumber": "992",
"StrengthUnit": "mL/L",
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20171231"
},
{
"NDCCode": "10702-006-01",
"PackageDescription": "100 TABLET, FILM COATED in 1 BOTTLE (10702-006-01) ",
"NDC11Code": "10702-0006-01",
"ProductNDC": "10702-006",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Cyclobenzaprine Hydrochloride",
"NonProprietaryName": "Cyclobenzaprine Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20140731",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078048",
"LabelerName": "KVK-TECH, Inc.",
"SubstanceName": "CYCLOBENZAPRINE HYDROCHLORIDE",
"StrengthNumber": "5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]",
"Status": "Active",
"LastUpdate": "2018-12-28",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20140731",
"SamplePackage": "N",
"IndicationAndUsage": "Cyclobenzaprine hydrochloride tablets, USP is indicated as an adjunct to rest and physical therapy for relief of muscle spasm associated with acute, painful musculoskeletal conditions. Improvement is manifested by relief of muscle spasm and its associated signs and symptoms, namely, pain, tenderness, limitation of motion, and restriction in activities of daily living. Cyclobenzaprine hydrochloride tablets, USP should be used only for short periods (up to two or three weeks) because adequate evidence of effectiveness for more prolonged use is not available and because muscle spasm associated with acute, painful musculoskeletal conditions is generally of short duration and specific therapy for longer periods is seldom warranted. Cyclobenzaprine hydrochloride tablets, USP have not been found effective in the treatment of spasticity associated with cerebral or spinal cord disease, or in children with cerebral palsy.",
"Description": "Cyclobenzaprine hydrochloride is a white, crystalline tricyclic amine salt with the empirical formula C 20H 21N HCl and a molecular weight of 311.9. It has a melting point of 217°C and a pKa of 8.47 at 25°C. It is freely soluble in water and alcohol, sparingly soluble in isopropanol, and insoluble in hydrocarbon solvents. If aqueous solutions are made alkaline, the free base separates. Cyclobenzaprine hydrochloride is designated chemically as 3-(5H-dibenzo [a,d] cyclohepten-5-ylidene)-N,N-dimethyl-1-propanamine hydrochloride, and has the following structural formula. Each 5 mg Cyclobenzaprine hydrochloride tablet for oral administration contains 5 mg Cyclobenzaprine hydrochloride. Each 10 mg Cyclobenzaprine hydrochloride tablet for oral administration contains 10 mg Cyclobenzaprine hydrochloride. Each tablet contains the following inactive ingredients: lactose monohydrate, microcrystalline cellulose, croscarmellose sodium, silicon dioxide, magnesium stearate, carnauba wax, titanium dioxide, polyethylene glycol, and iron oxide yellow. In addition, 5 mg tablets also contain polyvinyl alcohol, talc, lecithin, and FD&C yellow # 6 / sunset yellow FCF aluminum lake. In addition, 10 mg tablets also contain D&C yellow # 10 aluminum lake, FD&C yellow # 6 aluminum lake and hypromellose."
},
{
"NDCCode": "10812-006-01",
"PackageDescription": "1 TUBE in 1 CARTON (10812-006-01) > 50 mL in 1 TUBE",
"NDC11Code": "10812-0006-01",
"ProductNDC": "10812-006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Neutrogena Healthy Defense Spf30",
"NonProprietaryName": "Titanium Dioxide And Zinc Oxide",
"DosageFormName": "LOTION",
"RouteName": "TOPICAL",
"StartMarketingDate": "20091201",
"EndMarketingDate": "20150102",
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part352",
"LabelerName": "Neutrogena Corporation",
"SubstanceName": "TITANIUM DIOXIDE; ZINC OXIDE",
"StrengthNumber": "50; 30",
"StrengthUnit": "mg/mL; mg/mL",
"Status": "Deprecated",
"LastUpdate": "2015-01-09"
},
{
"NDCCode": "11054-006-01",
"PackageDescription": "85 L in 1 CYLINDER (11054-006-01) ",
"NDC11Code": "11054-0006-01",
"ProductNDC": "11054-006",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Nitrogen, Refrigerated",
"NonProprietaryName": "Nitrogen, Refrigerated",
"DosageFormName": "LIQUID",
"RouteName": "CUTANEOUS",
"StartMarketingDate": "19971106",
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA205839",
"LabelerName": "Airgas Usa, LLC",
"SubstanceName": "NITROGEN",
"StrengthNumber": "992",
"StrengthUnit": "mL/L",
"Status": "Active",
"LastUpdate": "2026-06-16",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "19971106",
"SamplePackage": "N"
},
{
"NDCCode": "11084-006-01",
"PackageDescription": "47 mL in 1 BOTTLE, PLASTIC (11084-006-01) ",
"NDC11Code": "11084-0006-01",
"ProductNDC": "11084-006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Alcare Extra Hand Sanitizer",
"NonProprietaryName": "Alcohol",
"DosageFormName": "SOLUTION",
"RouteName": "TOPICAL",
"StartMarketingDate": "20170301",
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "505G(a)(3)",
"LabelerName": "SC Johnson Professional USA, Inc.",
"SubstanceName": "ALCOHOL",
"StrengthNumber": "80",
"StrengthUnit": "mL/100mL",
"Status": "Active",
"LastUpdate": "2025-10-08",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20170301",
"SamplePackage": "N",
"IndicationAndUsage": "for hand sanitizing to reduce bacteria on the skin."
},
{
"NDCCode": "11324-006-01",
"PackageDescription": "8778 L in 1 CYLINDER (11324-006-01) ",
"NDC11Code": "11324-0006-01",
"ProductNDC": "11324-006",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Air",
"NonProprietaryName": "Air",
"DosageFormName": "GAS",
"RouteName": "RESPIRATORY (INHALATION)",
"StartMarketingDate": "20051001",
"MarketingCategoryName": "UNAPPROVED MEDICAL GAS",
"LabelerName": "Linde Puerto Rico B.V.",
"SubstanceName": "OXYGEN",
"StrengthNumber": "210",
"StrengthUnit": "mL/L",
"Status": "Active",
"LastUpdate": "2026-01-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20051001",
"SamplePackage": "N"
},
{
"NDCCode": "11559-006-01",
"PackageDescription": "1 TUBE in 1 CARTON (11559-006-01) > 30 mL in 1 TUBE (11559-006-02)",
"NDC11Code": "11559-0006-01",
"ProductNDC": "11559-006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Cyber White",
"ProprietaryNameSuffix": "Brilliant Cells Full Spectrum Brightening Uv Protector Spf 50",
"NonProprietaryName": "Homosalate, Octisalate, Avobenzone, Oxybenzone",
"DosageFormName": "LOTION",
"RouteName": "TOPICAL",
"StartMarketingDate": "20100601",
"MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
"ApplicationNumber": "part352",
"LabelerName": "ESTEE LAUDER INC",
"SubstanceName": "HOMOSALATE; OCTISALATE; AVOBENZONE; OXYBENZONE",
"StrengthNumber": "5; 5; 3; 3",
"StrengthUnit": "mL/100mL; mL/100mL; mL/100mL; mL/100mL",
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20171231"
},
{
"NDCCode": "11673-006-01",
"PackageDescription": "10 BLISTER PACK in 1 CARTON (11673-006-01) > 2 TABLET, FILM COATED in 1 BLISTER PACK",
"NDC11Code": "11673-0006-01",
"ProductNDC": "11673-006",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Up And Up Fast Mucus Relief Severe Cold",
"NonProprietaryName": "Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20150316",
"EndMarketingDate": "20211216",
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part341",
"LabelerName": "Target Corporation",
"SubstanceName": "ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE",
"StrengthNumber": "325; 10; 200; 5",
"StrengthUnit": "mg/1; mg/1; mg/1; mg/1",
"Status": "Deprecated",
"LastUpdate": "2021-12-17",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"StartMarketingDatePackage": "20150316",
"EndMarketingDatePackage": "20211216",
"SamplePackage": "N"
},
{
"NDCCode": "11994-006-02",
"PackageDescription": "2 KIT in 1 PACKAGE, COMBINATION (11994-006-02) > 1 KIT in 1 KIT * 1 INJECTION in 1 VIAL (11994-002-01) * 1 mL in 1 VIAL (11994-004-01) ",
"NDC11Code": "11994-0006-02",
"ProductNDC": "11994-006",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Neurolite",
"NonProprietaryName": "Bicisate Dihydrochloride",
"DosageFormName": "KIT",
"StartMarketingDate": "19941123",
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA020256",
"LabelerName": "Lantheus Medical Imaging, Inc.",
"Status": "Active",
"LastUpdate": "2022-11-29",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "19941123",
"SamplePackage": "N",
"IndicationAndUsage": "Neurolite single photon emission computerized tomography (SPECT) is indicated as an adjunct to conventional CT or MRI imaging in the localization of stroke in patients in whom stroke has already been diagnosed. Neurolite is not indicated for assessment of functional viability of brain tissue. Also, Neurolite is not indicated for distinguishing between stroke and other brain lesions.",
"Description": "This kit formulation consists of two nonradioactive vials: Vial A contains bicisate dihydrochloride (N, N'-1,2-ethylenediylbis-L-cysteine diethyl ester dihydrochloride) and a reducing agent as a lyophilized solid and vial B contains a buffer solution. Both vials are sterile and non-pyrogenic. The contents of vial A are lyophilized and stored under nitrogen. The pH of the solution before lyophilization is 2.7 ± 0.25. This vial is stored at 15-25°C. Protect from light. The contents of vial B are stored under air. The pH of the solution is 7.6 ± 0.4. This vial is stored at 15-25°C. This drug is administered by intravenous injection for diagnostic use after reconstitution with sterile, non-pyrogenic, oxidant-free Sodium Pertechnetate Tc99m Injection. The precise structure of the Technetium complex is [N, N'-ethylenedi-L-cysteinato(3-)]oxo[99mTc] technetium (V), diethyl ester."
},
{
"NDCCode": "11994-006-05",
"PackageDescription": "5 KIT in 1 PACKAGE, COMBINATION (11994-006-05) > 1 KIT in 1 KIT * 1 INJECTION in 1 VIAL (11994-002-01) * 1 mL in 1 VIAL (11994-004-01) ",
"NDC11Code": "11994-0006-05",
"ProductNDC": "11994-006",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Neurolite",
"NonProprietaryName": "Bicisate Dihydrochloride",
"DosageFormName": "KIT",
"StartMarketingDate": "19941123",
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA020256",
"LabelerName": "Lantheus Medical Imaging, Inc.",
"Status": "Active",
"LastUpdate": "2022-11-29",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "19941123",
"SamplePackage": "N",
"IndicationAndUsage": "Neurolite single photon emission computerized tomography (SPECT) is indicated as an adjunct to conventional CT or MRI imaging in the localization of stroke in patients in whom stroke has already been diagnosed. Neurolite is not indicated for assessment of functional viability of brain tissue. Also, Neurolite is not indicated for distinguishing between stroke and other brain lesions.",
"Description": "This kit formulation consists of two nonradioactive vials: Vial A contains bicisate dihydrochloride (N, N'-1,2-ethylenediylbis-L-cysteine diethyl ester dihydrochloride) and a reducing agent as a lyophilized solid and vial B contains a buffer solution. Both vials are sterile and non-pyrogenic. The contents of vial A are lyophilized and stored under nitrogen. The pH of the solution before lyophilization is 2.7 ± 0.25. This vial is stored at 15-25°C. Protect from light. The contents of vial B are stored under air. The pH of the solution is 7.6 ± 0.4. This vial is stored at 15-25°C. This drug is administered by intravenous injection for diagnostic use after reconstitution with sterile, non-pyrogenic, oxidant-free Sodium Pertechnetate Tc99m Injection. The precise structure of the Technetium complex is [N, N'-ethylenedi-L-cysteinato(3-)]oxo[99mTc] technetium (V), diethyl ester."
},
{
"NDCCode": "12121-006-01",
"PackageDescription": "361 L in 1 CYLINDER (12121-006-01)",
"NDC11Code": "12121-0006-01",
"ProductNDC": "12121-006",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Nitrogen",
"NonProprietaryName": "Nitrogen",
"DosageFormName": "GAS",
"RouteName": "RESPIRATORY (INHALATION)",
"StartMarketingDate": "19550101",
"MarketingCategoryName": "UNAPPROVED MEDICAL GAS",
"LabelerName": "Badger Welding Supplies, Inc",
"SubstanceName": "NITROGEN",
"StrengthNumber": "99",
"StrengthUnit": "L/100L",
"Status": "Deprecated",
"LastUpdate": "2014-11-14"
},
{
"NDCCode": "13107-006-01",
"PackageDescription": "100 TABLET in 1 BOTTLE (13107-006-01)",
"NDC11Code": "13107-0006-01",
"ProductNDC": "13107-006",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Citalopram",
"NonProprietaryName": "Citalopram",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20090101",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077031",
"LabelerName": "Aurolife Pharma LLC",
"SubstanceName": "CITALOPRAM HYDROBROMIDE",
"StrengthNumber": "20",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]",
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20181231",
"IndicationAndUsage": "A major depressive episode (DSM-IV) implies a prominent and relatively persistent (nearly every day for at least 2 weeks) depressed or dysphoric mood that usually interferes with daily functioning, and includes at least five of the following nine symptoms: depressed mood, loss of interest in usual activities, significant change in weight and/or appetite, insomnia or hypersomnia, psychomotor agitation or retardation, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, a suicide attempt or suicidal ideation. The antidepressant action of citalopram tablets, USP in hospitalized depressed patients has not been adequately studied.",
"Description": "Citalopram hydrobromide USP occurs as a fine, white to off-white powder. Citalopram hydrobromide is sparingly soluble in water and soluble in ethanol."
}
]
}
{"NDC":[{"NDCCode":"55146-006-01","ProprietaryName":"6 Environmental Detox","NonProprietaryName":"Baptisia Tinctoria, Phytolacca Decandra, Spigelia Anthelmia, Adrenocorticotrophin, Aluminum Metallicum, Apis Mellifica, Argentum Nitricum, Arsenicum Album, Benzoicum Acidum, Calcarea Carbonica, Carbo Vegetabilis, Kali Phosphoricum, Magnesia Sulphurica, Mercurius Solubilis, Nitricum Acidum, Nux Vomica, Phosphorus, Silicea"},{"NDCCode":"55146-001-01","ProprietaryName":"1 Detoxification","NonProprietaryName":"Capsicum Annuum, Phytolacca Decandra, Trifolium Pratense, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium Metallicum, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Oxydatum, Ferrum Metallicum, Gadolinium Oxydatum, Germanium Sesquioxide, Holmium,"},{"NDCCode":"55146-002-01","ProprietaryName":"2 Lymphatic Drainage","NonProprietaryName":"Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, Collinsonia Canadensis, Solidago Virgaurea, Hydrastis Canadensis, Fel Tauri, Apis Mellifica, Baryta Muriatica, Ceanothus Americanus, Chininum Sulphuricum, Conium Maculatum, Iodium, Lachesis Mutus, Mercurius Solubilis, Nux Vomica, Phosphorus, Silicea"},{"NDCCode":"55146-003-01","ProprietaryName":"3 Acute Stress","NonProprietaryName":"Arnica Montana, Bellis Perennis, Passiflora Incarnata, Valeriana Officinalis, Arsenicum Album, Apis Mellifica, Carcinosin, Cistus Canadensis, Clematis Erecta, Coffea Cruda, Ignatia Amara, Lachesis Mutus, Magnesia Phosphorica, Natrum Muriaticum, Natrum Sulphuricum, Ornithogalum Umbellatum, Phosphoricum Acidum, Salix Nigra, Staphysagria"},{"NDCCode":"55146-004-01","ProprietaryName":"4 Detox-virus","NonProprietaryName":"Astragalus Membranaceus, Baptisia Tinctoria, Echinacea (echinacea), Phytolacca Decandra, Hydrastis Canadensis, Apis Mellifica, Aranea Diadema, Belladonna, Eupatorium Perfoliatum, Gelsemium Sempervirens, Lachesis Mutus, Phosphoricum Acidum, Silicea, Thuja Occidentalis, Vaccinium Myrtillus"},{"NDCCode":"55146-005-01","ProprietaryName":"5 Chronic Stress","NonProprietaryName":"Aralia Quinquefolia, Fucus Vesiculosus, Solidago Virgaurea, Taraxacum Officinale, Trifolium Pratense, Hydrastis Canadensis, Arsenicum Album, Calcarea Carbonica, Carbo Vegetabilis, Ceanothus Americanus, Cyclamen Europaeum, Hepar Sulphuris Calcareum, Natrum Muriaticum, Nux Vomica, Petroleum, Phosphorus"},{"NDCCode":"55146-007-01","ProprietaryName":"7 Heavy Metal Detox","NonProprietaryName":"Allium Sativum, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Metallicum, Ferrum Metallicum, Gadolinium Metallicum, Germanium Sesquioxide, Holmium Metallicum, Indium Metallicum, Lithium Carbonicum, Magnesium Metallicum,"},{"NDCCode":"55146-008-01","ProprietaryName":"8 Fungal Yeast Infection","NonProprietaryName":"Astragalus Membranaceus, Berberis Vulgaris, Echinacea (angustifolia), Gentiana Lutea, Phytolacca Decandra, Hydrastis Canadensis, Candida Albicans, Apis Mellifica, Calcarea Carbonica, Lycopodium Clavatum, Mercurius Solubilis, Pulsatilla (vulgaris) Sepia, Thuja Occidentalis"},{"NDCCode":"55146-009-01","ProprietaryName":"9 Bacterial Detox","NonProprietaryName":"Baptisia Tinctoria, Dulcamara, Echinacea (angustifolia), Allium Sativum, Phytolacca Decandra, Apis Mellifica, Arsenicum Album, Belladonna, Chamomilla, Ferrum Phosphoricum, Gelsemium Sempervirens, Lachesis Mutus, Mercurius Solubilis, Pyrogenium"},{"NDCCode":"55146-010-01","ProprietaryName":"10 Parasite Detox","NonProprietaryName":"Carduus Marianus, Chelidonium Majus, Cina, Sabadilla, Teucrium Marum, Terebinthina, Thyroidinum (suis), Spigelia Anthelmia, Apis Mellifica, Baryta Carbonica, Calcarea Carbonica, Ferrum Muriaticum, Natrum Muriaticum, Silicea, Sulphur"},{"NDCCode":"55146-011-01","ProprietaryName":"1 Detoxification","NonProprietaryName":"Trifolium Pratense, Capsicum Annuum, Phytolacca Decandra, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Oxydatum, Ferrum Metallicum, Gadolinium Metallicum, Germanium Sesquioxide, Holmium Metallicum, Indium Metallicum,"},{"NDCCode":"10014-006-01","ProprietaryName":"Oxygen Helium Mixture","NonProprietaryName":"Oxygen Helium Mixture"},{"NDCCode":"10056-006-01","ProprietaryName":"Satinique Anti Dandruff","NonProprietaryName":"Pyrithione Zinc"},{"NDCCode":"10095-006-01","ProprietaryName":"Quitacallos","NonProprietaryName":"Salicylic Acid"},{"NDCCode":"10297-006-01","ProprietaryName":"Helium","NonProprietaryName":"Helium"},{"NDCCode":"10348-006-01","ProprietaryName":"Smashbox","NonProprietaryName":"Avobenzone, Homosalate, And Octisalate"},{"NDCCode":"10526-006-01","ProprietaryName":"Nitrogen","NonProprietaryName":"Nitrogen"},{"NDCCode":"10578-006-01","ProprietaryName":"Homeopathic Scar","NonProprietaryName":"Pot Marigold, Bushmaster Snake, Black Lead, Oil Of Mustard Seed"},{"NDCCode":"10678-006-01","ProprietaryName":"Nitrous Oxide","NonProprietaryName":"Nitrous Oxide"},{"NDCCode":"10702-006-01","ProprietaryName":"Cyclobenzaprine Hydrochloride","NonProprietaryName":"Cyclobenzaprine Hydrochloride"},{"NDCCode":"10812-006-01","ProprietaryName":"Neutrogena Healthy Defense Spf30","NonProprietaryName":"Titanium Dioxide And Zinc Oxide"},{"NDCCode":"11054-006-01","ProprietaryName":"Nitrogen, Refrigerated","NonProprietaryName":"Nitrogen, Refrigerated"},{"NDCCode":"11084-006-01","ProprietaryName":"Alcare Extra Hand Sanitizer","NonProprietaryName":"Alcohol"},{"NDCCode":"11324-006-01","ProprietaryName":"Air","NonProprietaryName":"Air"},{"NDCCode":"11559-006-01","ProprietaryName":"Cyber White","NonProprietaryName":"Homosalate, Octisalate, Avobenzone, Oxybenzone"},{"NDCCode":"11673-006-01","ProprietaryName":"Up And Up Fast Mucus Relief Severe Cold","NonProprietaryName":"Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl"},{"NDCCode":"11994-006-02","ProprietaryName":"Neurolite","NonProprietaryName":"Bicisate Dihydrochloride"},{"NDCCode":"11994-006-05","ProprietaryName":"Neurolite","NonProprietaryName":"Bicisate Dihydrochloride"},{"NDCCode":"12121-006-01","ProprietaryName":"Nitrogen","NonProprietaryName":"Nitrogen"},{"NDCCode":"13107-006-01","ProprietaryName":"Citalopram","NonProprietaryName":"Citalopram"}]}
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<NDCList>
<NDC>
<NDCCode>55146-006-01</NDCCode>
<PackageDescription>120 mL in 1 BOTTLE, PLASTIC (55146-006-01) </PackageDescription>
<NDC11Code>55146-0006-01</NDC11Code>
<ProductNDC>55146-006</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>6 Environmental Detox</ProprietaryName>
<NonProprietaryName>Baptisia Tinctoria, Phytolacca Decandra, Spigelia Anthelmia, Adrenocorticotrophin, Aluminum Metallicum, Apis Mellifica, Argentum Nitricum, Arsenicum Album, Benzoicum Acidum, Calcarea Carbonica, Carbo Vegetabilis, Kali Phosphoricum, Magnesia Sulphurica, Mercurius Solubilis, Nitricum Acidum, Nux Vomica, Phosphorus, Silicea</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20190611</StartMarketingDate>
<EndMarketingDate>20251211</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Biotics Research Corporation</LabelerName>
<SubstanceName>ACTIVATED CHARCOAL; ALUMINUM; APIS MELLIFERA; ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BENZOIC ACID; CORTICOTROPIN; MAGNESIUM SULFATE HEPTAHYDRATE; MERCURIUS SOLUBILIS; NITRIC ACID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; POTASSIUM PHOSPHATE, DIBASIC; SILICON DIOXIDE; SILVER NITRATE; SPIGELIA ANTHELMIA WHOLE; STRYCHNOS NUX-VOMICA SEED</SubstanceName>
<StrengthNumber>30; 30; 30; 30; 3; 30; 30; 30; 30; 30; 30; 30; 4; 30; 30; 30; 6; 30</StrengthNumber>
<StrengthUnit>[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL</StrengthUnit>
<Pharm_Classes>Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Allergens [CS], Ammonium Ion Binding Activity [MoA], Bee Venoms [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Nitrogen Binding Agent [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2025-12-16</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20190611</StartMarketingDatePackage>
<EndMarketingDatePackage>20251211</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For temporary relief of cough, rattling in chest, hoarseness, sore throat, skin irritation and vomiting upon environmental exposure. Remedy # 6 supports detoxification of insecticides, environmental and industrial pollutants.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>55146-001-01</NDCCode>
<PackageDescription>120 mL in 1 BOTTLE (55146-001-01) </PackageDescription>
<NDC11Code>55146-0001-01</NDC11Code>
<ProductNDC>55146-001</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>1 Detoxification</ProprietaryName>
<NonProprietaryName>Capsicum Annuum, Phytolacca Decandra, Trifolium Pratense, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium Metallicum, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Oxydatum, Ferrum Metallicum, Gadolinium Oxydatum, Germanium Sesquioxide, Holmium,</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20190610</StartMarketingDate>
<EndMarketingDate>20250625</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Biotics Research Corporation</LabelerName>
<SubstanceName>ACTIVATED CHARCOAL; ALCOHOL, X-RAY EXPOSED (1000 RAD); ALLYLTHIOUREA; ALUMINUM; ANGUILLA ROSTRATA BLOOD SERUM; ANTIMONY TRISULFIDE; APIS MELLIFERA; ARSENIC TRIOXIDE; BACILLUS ANTHRACIS IMMUNOSERUM RABBIT; BARIUM CARBONATE; BERYLLIUM; BISMUTH; BORON; BROMINE; CADMIUM; CAPSICUM; CARBO ANIMALIS; CERIUM; CESIUM CHLORIDE; CHROMIUM; CLAVICEPS PURPUREA SCLEROTIUM; COBALT; CONIUM MACULATUM FLOWERING TOP; COPPER; CORTICOTROPIN; DYSPROSIUM; ERBIUM; EUROPIUM; GADOLINIUM; GELSEMIUM SEMPERVIRENS ROOT; GERMANIUM SESQUIOXIDE; GOLD; HOLMIUM; HUMAN BREAST TUMOR CELL; INDIUM; IRON; LACHESIS MUTA VENOM; LANTHANUM; LEAD; LITHIUM CARBONATE; MAGNESIUM; MANGANESE; MERCURIUS SOLUBILIS; MOLYBDENUM; NEODYMIUM OXIDE; NICKEL; NIOBIUM; OSMIUM; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PALLADIUM; PHOSPHORIC ACID; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PLATINUM; POTASSIUM DICHROMATE; PRASEODYMIUM; RANCID BEEF; RHODIUM; RUBIDIUM NITRITE; SAMARIUM; SELENIUM; SILVER; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRONTIUM CARBONATE; STRYCHNOS WALLICHIANA BARK; SULFURIC ACID; SUS SCROFA PITUITARY GLAND; TANTALUM; TARTARIC ACID; TERBIUM; THALLIUM; THERIDION CURASSAVICUM; THUJA OCCIDENTALIS LEAFY TWIG; THYROID; TIN; TRIFOLIUM PRATENSE FLOWER; URANYL NITRATE HEXAHYDRATE; VANADIUM; VERATRUM ALBUM ROOT; YTTERBIUM OXIDE; ZINC</SubstanceName>
<StrengthNumber>30; 30; 30; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 30; 12; 3; 30; 12; 12; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 30; 12; 12; 12; 30; 12; 12; 30; 14; 12; 12; 12; 12; 12; 12; 12; 12; 30; 12; 30; 12; 30; 30; 4; 12; 30; 12; 30; 12; 12; 12; 12; 12; 30; 12; 30; 30; 30; 30; 30; 12; 12; 30; 30; 30; 12; 3; 12; 12; 30; 12; 12</StrengthNumber>
<StrengthUnit>[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_X]/mL; [hp_C]/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_C]/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_C]/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_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/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_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/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_C]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Mood Stabilizer [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2025-06-26</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20190610</StartMarketingDatePackage>
<EndMarketingDatePackage>20250625</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For temporary relief of gastrointestinal dyspepsia (indigestion) with flatulence, bloating and intolerance of certain foods. Remedy #1 supports detoxification and cellular repair.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>55146-002-01</NDCCode>
<PackageDescription>120 mL in 1 BOTTLE, PLASTIC (55146-002-01) </PackageDescription>
<NDC11Code>55146-0002-01</NDC11Code>
<ProductNDC>55146-002</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>2 Lymphatic Drainage</ProprietaryName>
<NonProprietaryName>Berberis Vulgaris, Carduus Marianus, Chelidonium Majus, Collinsonia Canadensis, Solidago Virgaurea, Hydrastis Canadensis, Fel Tauri, Apis Mellifica, Baryta Muriatica, Ceanothus Americanus, Chininum Sulphuricum, Conium Maculatum, Iodium, Lachesis Mutus, Mercurius Solubilis, Nux Vomica, Phosphorus, Silicea</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20190611</StartMarketingDate>
<EndMarketingDate>20250821</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Biotics Research Corporation</LabelerName>
<SubstanceName>APIS MELLIFERA; BARIUM CHLORIDE DIHYDRATE; BERBERIS VULGARIS ROOT BARK; BOS TAURUS BILE; CEANOTHUS AMERICANUS LEAF; CHELIDONIUM MAJUS; COLLINSONIA CANADENSIS ROOT; CONIUM MACULATUM FLOWERING TOP; GOLDENSEAL; IODINE; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; MILK THISTLE; PHOSPHORUS; QUININE SULFATE; SILICON DIOXIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; STRYCHNOS NUX-VOMICA SEED</SubstanceName>
<StrengthNumber>30; 30; 3; 6; 30; 3; 3; 30; 5; 30; 30; 30; 3; 30; 30; 30; 3; 30</StrengthNumber>
<StrengthUnit>[hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL</StrengthUnit>
<Pharm_Classes>Allergens [CS], Allergens [CS], Antimalarial [EPC], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2025-08-22</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20190611</StartMarketingDatePackage>
<EndMarketingDatePackage>20250821</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For temporary relief of fever, sore throat and acute irritation of the bladder. Remedy #2 supports the clearing of organs allowing for lymphatic drainage and detoxification of any stored toxins that have been released during the cleansing.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>55146-003-01</NDCCode>
<PackageDescription>120 mL in 1 BOTTLE, PLASTIC (55146-003-01) </PackageDescription>
<NDC11Code>55146-0003-01</NDC11Code>
<ProductNDC>55146-003</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>3 Acute Stress</ProprietaryName>
<NonProprietaryName>Arnica Montana, Bellis Perennis, Passiflora Incarnata, Valeriana Officinalis, Arsenicum Album, Apis Mellifica, Carcinosin, Cistus Canadensis, Clematis Erecta, Coffea Cruda, Ignatia Amara, Lachesis Mutus, Magnesia Phosphorica, Natrum Muriaticum, Natrum Sulphuricum, Ornithogalum Umbellatum, Phosphoricum Acidum, Salix Nigra, Staphysagria</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20190611</StartMarketingDate>
<EndMarketingDate>20250716</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Biotics Research Corporation</LabelerName>
<SubstanceName>APIS MELLIFERA; ARABICA COFFEE BEAN; ARNICA MONTANA WHOLE; ARSENIC TRIOXIDE; BELLIS PERENNIS WHOLE; CLEMATIS RECTA FLOWERING TOP; DELPHINIUM STAPHISAGRIA SEED; HELIANTHEMUM CANADENSE; HUMAN BREAST TUMOR CELL; LACHESIS MUTA VENOM; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; ORNITHOGALUM UMBELLATUM WHOLE; PASSIFLORA INCARNATA FLOWERING TOP; PHOSPHORIC ACID; SALIX NIGRA BARK; SODIUM CHLORIDE; SODIUM SULFATE; STRYCHNOS IGNATII SEED; VALERIAN</SubstanceName>
<StrengthNumber>30; 30; 3; 6; 3; 30; 30; 30; 30; 30; 30; 30; 3; 30; 30; 30; 30; 30; 3</StrengthNumber>
<StrengthUnit>[hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Allergens [CS], Allergens [CS], Bee Venoms [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2025-07-17</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20190611</StartMarketingDatePackage>
<EndMarketingDatePackage>20250716</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For temporary relief of acute stress due to emotional strain, anxiety, sleeplessness, apprehension or fear.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>55146-004-01</NDCCode>
<PackageDescription>120 mL in 1 BOTTLE, PLASTIC (55146-004-01) </PackageDescription>
<NDC11Code>55146-0004-01</NDC11Code>
<ProductNDC>55146-004</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>4 Detox-virus</ProprietaryName>
<NonProprietaryName>Astragalus Membranaceus, Baptisia Tinctoria, Echinacea (echinacea), Phytolacca Decandra, Hydrastis Canadensis, Apis Mellifica, Aranea Diadema, Belladonna, Eupatorium Perfoliatum, Gelsemium Sempervirens, Lachesis Mutus, Phosphoricum Acidum, Silicea, Thuja Occidentalis, Vaccinium Myrtillus</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20190611</StartMarketingDate>
<EndMarketingDate>20250625</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Biotics Research Corporation</LabelerName>
<SubstanceName>APIS MELLIFERA; ARANEUS DIADEMATUS; ARSENIC TRIOXIDE; ASTRAGALUS PROPINQUUS ROOT; ATROPA BELLADONNA; BAPTISIA TINCTORIA; BILBERRY; ECHINACEA ANGUSTIFOLIA WHOLE; EUPATORIUM PERFOLIATUM FLOWERING TOP; GELSEMIUM SEMPERVIRENS ROOT; GOLDENSEAL; LACHESIS MUTA VENOM; PHOSPHORIC ACID; PHYTOLACCA AMERICANA ROOT; RANCID BEEF; SILICON DIOXIDE; THUJA OCCIDENTALIS LEAFY TWIG</SubstanceName>
<StrengthNumber>30; 30; 30; 3; 30; 3; 30; 3; 30; 30; 5; 30; 30; 4; 30; 30; 30</StrengthNumber>
<StrengthUnit>[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL</StrengthUnit>
<Pharm_Classes>Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2025-06-26</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20190611</StartMarketingDatePackage>
<EndMarketingDatePackage>20250625</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For temporary relief of skin irritation, dry cough, eczema or fever. Remedy #4 supports detoxification of residual toxins left from a viral infection.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>55146-005-01</NDCCode>
<PackageDescription>120 mL in 1 BOTTLE, PLASTIC (55146-005-01) </PackageDescription>
<NDC11Code>55146-0005-01</NDC11Code>
<ProductNDC>55146-005</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>5 Chronic Stress</ProprietaryName>
<NonProprietaryName>Aralia Quinquefolia, Fucus Vesiculosus, Solidago Virgaurea, Taraxacum Officinale, Trifolium Pratense, Hydrastis Canadensis, Arsenicum Album, Calcarea Carbonica, Carbo Vegetabilis, Ceanothus Americanus, Cyclamen Europaeum, Hepar Sulphuris Calcareum, Natrum Muriaticum, Nux Vomica, Petroleum, Phosphorus</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20190611</StartMarketingDate>
<EndMarketingDate>20250701</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Biotics Research Corporation</LabelerName>
<SubstanceName>ACTIVATED CHARCOAL; AMERICAN GINSENG; ARSENIC TRIOXIDE; CEANOTHUS AMERICANUS LEAF; CYCLAMEN PURPURASCENS TUBER; FUCUS VESICULOSUS; GOLDENSEAL; KEROSENE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHOSPHORUS; SODIUM CHLORIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; STRYCHNOS NUX-VOMICA SEED; TARAXACUM OFFICINALE; TRIFOLIUM PRATENSE FLOWER</SubstanceName>
<StrengthNumber>30; 3; 30; 30; 30; 3; 5; 30; 30; 30; 30; 3; 30; 3; 3</StrengthNumber>
<StrengthUnit>[hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Seed Storage Proteins [CS]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2025-07-01</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20190611</StartMarketingDatePackage>
<EndMarketingDatePackage>20250701</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For temporary relief of debility or exhaustion after slight exertion, or exhaustion following dysentery. Remedy #5 supports the easing of chronic stress produced by natural substances called adaptogens.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>55146-007-01</NDCCode>
<PackageDescription>120 mL in 1 BOTTLE, PLASTIC (55146-007-01) </PackageDescription>
<NDC11Code>55146-0007-01</NDC11Code>
<ProductNDC>55146-007</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>7 Heavy Metal Detox</ProprietaryName>
<NonProprietaryName>Allium Sativum, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Metallicum, Ferrum Metallicum, Gadolinium Metallicum, Germanium Sesquioxide, Holmium Metallicum, Indium Metallicum, Lithium Carbonicum, Magnesium Metallicum,</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20190611</StartMarketingDate>
<EndMarketingDate>20250625</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Biotics Research Corporation</LabelerName>
<SubstanceName>ALUMINUM; ANTIMONY TRISULFIDE; APIS MELLIFERA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BARIUM CARBONATE; BERBERIS VULGARIS ROOT BARK; BERYLLIUM; BISMUTH; BORON; BROMINE; CADMIUM; CALCIUM SULFIDE; CAUSTICUM; CERIUM; CESIUM CHLORIDE; CHROMIUM; COBALT; CONIUM MACULATUM FLOWERING TOP; COPPER; DYSPROSIUM; ERBIUM; EUROPIUM OXIDE; GADOLINIUM; GARLIC; GERMANIUM SESQUIOXIDE; GOLD; HOLMIUM; HYPERICUM PERFORATUM; INDIUM; IPECAC; IRON; LANTHANUM; LEAD; LITHIUM CARBONATE; MAGNESIUM; MANGANESE; MERCURIUS SOLUBILIS; MOLYBDENUM; NEODYMIUM OXIDE; NICKEL; NIOBIUM; OSMIUM; PALLADIUM; PLATINUM; PRASEODYMIUM; RHODIUM; RUBIDIUM NITRITE; SAMARIUM; SELENIUM; SILVER; STRONTIUM CARBONATE; TANTALUM; TERBIUM; THALLIUM; TIN; URANYL NITRATE HEXAHYDRATE; VANADIUM; VERATRUM ALBUM ROOT; YTTERBIUM OXIDE; ZINC</SubstanceName>
<StrengthNumber>12; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 12; 30; 30; 12; 12; 12; 12; 30; 12; 12; 12; 12; 12; 4; 12; 12; 12; 30; 12; 30; 12; 14; 12; 12; 12; 12; 12; 12; 12; 12; 30; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 30; 12; 12; 12; 12; 12; 30; 12; 12</StrengthNumber>
<StrengthUnit>[hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/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_C]/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_C]/mL; [hp_X]/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_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_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</StrengthUnit>
<Pharm_Classes>Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Mood Stabilizer [EPC], Non-Standardized Food Allergenic Extract [EPC], Plant Proteins [CS], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2025-06-26</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20190611</StartMarketingDatePackage>
<EndMarketingDatePackage>20250625</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>Temporary relief of neurological disorders, vomiting, prostration and metallic aftertaste. Remedy #7 supports detoxification of environmental pollutants.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>55146-008-01</NDCCode>
<PackageDescription>120 mL in 1 BOTTLE, PLASTIC (55146-008-01) </PackageDescription>
<NDC11Code>55146-0008-01</NDC11Code>
<ProductNDC>55146-008</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>8 Fungal Yeast Infection</ProprietaryName>
<NonProprietaryName>Astragalus Membranaceus, Berberis Vulgaris, Echinacea (angustifolia), Gentiana Lutea, Phytolacca Decandra, Hydrastis Canadensis, Candida Albicans, Apis Mellifica, Calcarea Carbonica, Lycopodium Clavatum, Mercurius Solubilis, Pulsatilla (vulgaris) Sepia, Thuja Occidentalis</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20190611</StartMarketingDate>
<EndMarketingDate>20230413</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Biotics Research Corporation</LabelerName>
<SubstanceName>APIS MELLIFERA; ASTRAGALUS PROPINQUUS ROOT; BERBERIS VULGARIS ROOT BARK; CANDIDA ALBICANS; ECHINACEA ANGUSTIFOLIA; GENTIANA LUTEA ROOT; GOLDENSEAL; LYCOPODIUM CLAVATUM SPORE; MERCURIUS SOLUBILIS; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; SEPIA OFFICINALIS JUICE; THUJA OCCIDENTALIS LEAF</SubstanceName>
<StrengthNumber>30; 3; 3; 12; 3; 3; 5; 30; 30; 30; 4; 30; 30; 30</StrengthNumber>
<StrengthUnit>[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_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL</StrengthUnit>
<Pharm_Classes>Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Standardized Insect Venom Allergenic Extract [EPC]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2023-04-14</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20190611</StartMarketingDatePackage>
<EndMarketingDatePackage>20230413</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>55146-009-01</NDCCode>
<PackageDescription>120 mL in 1 BOTTLE, PLASTIC (55146-009-01) </PackageDescription>
<NDC11Code>55146-0009-01</NDC11Code>
<ProductNDC>55146-009</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>9 Bacterial Detox</ProprietaryName>
<NonProprietaryName>Baptisia Tinctoria, Dulcamara, Echinacea (angustifolia), Allium Sativum, Phytolacca Decandra, Apis Mellifica, Arsenicum Album, Belladonna, Chamomilla, Ferrum Phosphoricum, Gelsemium Sempervirens, Lachesis Mutus, Mercurius Solubilis, Pyrogenium</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20190611</StartMarketingDate>
<EndMarketingDate>20250625</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Biotics Research Corporation</LabelerName>
<SubstanceName>APIS MELLIFERA; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BAPTISIA TINCTORIA ROOT; ECHINACEA ANGUSTIFOLIA WHOLE; FERROSOFERRIC PHOSPHATE; GARLIC; GELSEMIUM SEMPERVIRENS ROOT; LACHESIS MUTA VENOM; MATRICARIA CHAMOMILLA WHOLE; MERCURIUS SOLUBILIS; PHYTOLACCA AMERICANA ROOT; RANCID BEEF; SOLANUM DULCAMARA TOP</SubstanceName>
<StrengthNumber>30; 30; 30; 3; 3; 30; 4; 30; 30; 30; 30; 4; 30; 3</StrengthNumber>
<StrengthUnit>[hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Plant Proteins [CS], Standardized Insect Venom Allergenic Extract [EPC]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2025-06-26</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20190611</StartMarketingDatePackage>
<EndMarketingDatePackage>20250625</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For temporary relief of fever, sore throat and acute irritation of the bladder. Remedy #9 supports detoxification of toxins that remain after a bacterial infection.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>55146-010-01</NDCCode>
<PackageDescription>120 mL in 1 BOTTLE, PLASTIC (55146-010-01) </PackageDescription>
<NDC11Code>55146-0010-01</NDC11Code>
<ProductNDC>55146-010</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>10 Parasite Detox</ProprietaryName>
<NonProprietaryName>Carduus Marianus, Chelidonium Majus, Cina, Sabadilla, Teucrium Marum, Terebinthina, Thyroidinum (suis), Spigelia Anthelmia, Apis Mellifica, Baryta Carbonica, Calcarea Carbonica, Ferrum Muriaticum, Natrum Muriaticum, Silicea, Sulphur</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20190611</StartMarketingDate>
<EndMarketingDate>20250625</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Biotics Research Corporation</LabelerName>
<SubstanceName>APIS MELLIFERA; ARTEMISIA CINA PRE-FLOWERING TOP; BARIUM CARBONATE; CHELIDONIUM MAJUS WHOLE; FERRIC CHLORIDE HEXAHYDRATE; MILK THISTLE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SCHOENOCAULON OFFICINALE SEED; SILICON DIOXIDE; SODIUM CHLORIDE; SPIGELIA ANTHELMIA WHOLE; SULFUR; TEUCRIUM MARUM WHOLE; THYROID; TURPENTINE OIL</SubstanceName>
<StrengthNumber>30; 3; 30; 3; 30; 3; 30; 3; 30; 30; 6; 30; 3; 6; 5</StrengthNumber>
<StrengthUnit>[hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/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</StrengthUnit>
<Pharm_Classes>Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Iron [CS], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Standardized Insect Venom Allergenic Extract [EPC]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2025-06-26</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20190611</StartMarketingDatePackage>
<EndMarketingDatePackage>20250625</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For temporary relief of fever, joint pain, cough, stiffness and gastric upset. Remedy #10 supports detoxification of toxins that remain following a parasitic infection.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>55146-011-01</NDCCode>
<PackageDescription>120 mL in 1 BOTTLE (55146-011-01) </PackageDescription>
<NDC11Code>55146-0011-01</NDC11Code>
<ProductNDC>55146-011</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>1 Detoxification</ProprietaryName>
<NonProprietaryName>Trifolium Pratense, Capsicum Annuum, Phytolacca Decandra, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Cerium Metallicum, Cesium Chloride, Chromium, Cobaltum Metallicum, Cuprum Metallicum, Dysprosium Metallicum, Erbium Metallicum, Europium Oxydatum, Ferrum Metallicum, Gadolinium Metallicum, Germanium Sesquioxide, Holmium Metallicum, Indium Metallicum,</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20200505</StartMarketingDate>
<EndMarketingDate>20250625</EndMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Biotics Research Corporation</LabelerName>
<SubstanceName>ACTIVATED CHARCOAL; ALCOHOL, X-RAY EXPOSED (1000 RAD); ALLYLTHIOUREA; ALUMINUM; ANGUILLA ROSTRATA BLOOD SERUM; ANTIMONY TRISULFIDE; APIS MELLIFERA; ARSENIC TRIOXIDE; BACILLUS ANTHRACIS IMMUNOSERUM RABBIT; BARIUM CARBONATE; BERYLLIUM; BISMUTH; BORON; BROMINE; CADMIUM; CAPSICUM; CARBO ANIMALIS; CERIUM; CESIUM CHLORIDE; CHROMIUM; CLAVICEPS PURPUREA SCLEROTIUM; COBALT; CONIUM MACULATUM FLOWERING TOP; COPPER; CORTICOTROPIN; DYSPROSIUM; ERBIUM; EUROPIUM; GADOLINIUM; GELSEMIUM SEMPERVIRENS ROOT; GERMANIUM SESQUIOXIDE; GOLD; HOLMIUM; HUMAN BREAST TUMOR CELL; INDIUM; IRON; LACHESIS MUTA VENOM; LANTHANUM; LEAD; LITHIUM CARBONATE; MAGNESIUM; MANGANESE; MERCURIUS SOLUBILIS; MOLYBDENUM; NEODYMIUM OXIDE; NICKEL; NIOBIUM; OSMIUM; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PALLADIUM; PHOSPHORIC ACID; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PLATINUM; POTASSIUM DICHROMATE; PRASEODYMIUM; RANCID BEEF; RHODIUM; RUBIDIUM NITRITE; SAMARIUM; SELENIUM; SILVER; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; STRONTIUM CARBONATE; STRYCHNOS WALLICHIANA BARK; SULFURIC ACID; SUS SCROFA PITUITARY GLAND; TANTALUM; TARTARIC ACID; TERBIUM; THALLIUM; THERIDION CURASSAVICUM; THUJA OCCIDENTALIS LEAFY TWIG; THYROID; TIN; TRIFOLIUM PRATENSE FLOWER; URANYL NITRATE HEXAHYDRATE; VANADIUM; VERATRUM ALBUM ROOT; YTTERBIUM OXIDE; ZINC</SubstanceName>
<StrengthNumber>30; 30; 30; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 12; 12; 3; 30; 12; 12; 12; 30; 12; 30; 12; 30; 12; 12; 12; 12; 30; 12; 12; 12; 30; 12; 12; 30; 14; 12; 12; 12; 12; 12; 12; 12; 12; 30; 12; 30; 12; 30; 30; 4; 12; 30; 12; 30; 12; 12; 12; 12; 12; 30; 12; 30; 30; 30; 30; 30; 12; 12; 30; 30; 30; 12; 3; 12; 12; 30; 12; 12</StrengthNumber>
<StrengthUnit>[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_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_C]/mL; [hp_X]/mL; [hp_C]/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_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_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/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_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/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_C]/mL; [hp_X]/mL; [hp_X]/mL</StrengthUnit>
<Pharm_Classes>Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Mood Stabilizer [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Insect Venom Allergenic Extract [EPC], Vegetable Proteins [CS]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2025-06-26</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20200505</StartMarketingDatePackage>
<EndMarketingDatePackage>20250625</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>For temporary relief of gastrointestinal dyspepsia (indigestion) with flatulence, bloating and intolerance of certain foods. Remedy #1 supports detoxification and cellular repair.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>10014-006-01</NDCCode>
<PackageDescription>113 L in 1 CYLINDER (10014-006-01)</PackageDescription>
<NDC11Code>10014-0006-01</NDC11Code>
<ProductNDC>10014-006</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Oxygen Helium Mixture</ProprietaryName>
<NonProprietaryName>Oxygen Helium Mixture</NonProprietaryName>
<DosageFormName>GAS</DosageFormName>
<RouteName>RESPIRATORY (INHALATION)</RouteName>
<StartMarketingDate>19721006</StartMarketingDate>
<MarketingCategoryName>UNAPPROVED MEDICAL GAS</MarketingCategoryName>
<LabelerName>Aero All Gas Company</LabelerName>
<SubstanceName>OXYGEN; HELIUM</SubstanceName>
<StrengthNumber>200; 800</StrengthNumber>
<StrengthUnit>mL/L; mL/L</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2019-09-21</LastUpdate>
<ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>10056-006-01</NDCCode>
<PackageDescription>280 mL in 1 BOTTLE (10056-006-01) </PackageDescription>
<NDC11Code>10056-0006-01</NDC11Code>
<ProductNDC>10056-006</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Satinique Anti Dandruff</ProprietaryName>
<NonProprietaryName>Pyrithione Zinc</NonProprietaryName>
<DosageFormName>CREAM</DosageFormName>
<RouteName>TOPICAL</RouteName>
<StartMarketingDate>20170329</StartMarketingDate>
<MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
<ApplicationNumber>M032</ApplicationNumber>
<LabelerName>Access Business Group LLC</LabelerName>
<SubstanceName>PYRITHIONE ZINC</SubstanceName>
<StrengthNumber>9.5</StrengthNumber>
<StrengthUnit>mg/mL</StrengthUnit>
<Status>Active</Status>
<LastUpdate>2023-10-24</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20170329</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>Controls symptoms of dandruff.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>10095-006-01</NDCCode>
<PackageDescription>15 g in 1 PACKAGE (10095-006-01)</PackageDescription>
<NDC11Code>10095-0006-01</NDC11Code>
<ProductNDC>10095-006</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Quitacallos</ProprietaryName>
<NonProprietaryName>Salicylic Acid</NonProprietaryName>
<DosageFormName>CREAM</DosageFormName>
<RouteName>TOPICAL</RouteName>
<StartMarketingDate>20150505</StartMarketingDate>
<MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
<ApplicationNumber>part358F</ApplicationNumber>
<LabelerName>World Perfumes, Inc</LabelerName>
<SubstanceName>SALICYLIC ACID</SubstanceName>
<StrengthNumber>17</StrengthNumber>
<StrengthUnit>g/100g</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2019-09-21</LastUpdate>
<ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
<IndicationAndUsage>QuitaCallos. Removedor de Callos. Corn & Callus Remover. Salicylic Acid 17%.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>10297-006-01</NDCCode>
<PackageDescription>85 L in 1 CYLINDER (10297-006-01) </PackageDescription>
<NDC11Code>10297-0006-01</NDC11Code>
<ProductNDC>10297-006</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Helium</ProprietaryName>
<NonProprietaryName>Helium</NonProprietaryName>
<DosageFormName>GAS</DosageFormName>
<RouteName>RESPIRATORY (INHALATION)</RouteName>
<StartMarketingDate>20180601</StartMarketingDate>
<MarketingCategoryName>NDA</MarketingCategoryName>
<ApplicationNumber>NDA211781</ApplicationNumber>
<LabelerName>A-OX Welding Supply, LLC</LabelerName>
<SubstanceName>HELIUM</SubstanceName>
<StrengthNumber>990</StrengthNumber>
<StrengthUnit>mL/L</StrengthUnit>
<Status>Active</Status>
<LastUpdate>2025-12-16</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20180601</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>10348-006-01</NDCCode>
<PackageDescription>1 TUBE in 1 CARTON (10348-006-01) > 50 mL in 1 TUBE</PackageDescription>
<NDC11Code>10348-0006-01</NDC11Code>
<ProductNDC>10348-006</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Smashbox</ProprietaryName>
<ProprietaryNameSuffix>Photo Finish Foundation Primer Spf 20</ProprietaryNameSuffix>
<NonProprietaryName>Avobenzone, Homosalate, And Octisalate</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>TOPICAL</RouteName>
<StartMarketingDate>20120527</StartMarketingDate>
<MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
<ApplicationNumber>part352</ApplicationNumber>
<LabelerName>SMASHBOX BEAUTY COSMETICS, INC</LabelerName>
<SubstanceName>AVOBENZONE; HOMOSALATE; OCTISALATE</SubstanceName>
<StrengthNumber>2; 15; 5</StrengthNumber>
<StrengthUnit>mL/100mL; mL/100mL; mL/100mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2019-09-21</LastUpdate>
<ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
<IndicationAndUsage>helps prevent sunburn.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>10526-006-01</NDCCode>
<PackageDescription>230 L in 1 DEWAR (10526-006-01) </PackageDescription>
<NDC11Code>10526-0006-01</NDC11Code>
<ProductNDC>10526-006</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Nitrogen</ProprietaryName>
<NonProprietaryName>Nitrogen</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>RESPIRATORY (INHALATION)</RouteName>
<StartMarketingDate>19900101</StartMarketingDate>
<MarketingCategoryName>NDA</MarketingCategoryName>
<ApplicationNumber>NDA205766</ApplicationNumber>
<LabelerName>Haun Welding Supply, Inc.</LabelerName>
<SubstanceName>NITROGEN</SubstanceName>
<StrengthNumber>990</StrengthNumber>
<StrengthUnit>mL/L</StrengthUnit>
<Status>Active</Status>
<LastUpdate>2025-12-30</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>19900101</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>10578-006-01</NDCCode>
<PackageDescription>28 g in 1 JAR (10578-006-01)</PackageDescription>
<NDC11Code>10578-0006-01</NDC11Code>
<ProductNDC>10578-006</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Homeopathic Scar</ProprietaryName>
<NonProprietaryName>Pot Marigold, Bushmaster Snake, Black Lead, Oil Of Mustard Seed</NonProprietaryName>
<DosageFormName>CREAM</DosageFormName>
<RouteName>TOPICAL</RouteName>
<StartMarketingDate>20120427</StartMarketingDate>
<MarketingCategoryName>UNAPPROVED HOMEOPATHIC</MarketingCategoryName>
<LabelerName>Indiana Botanic Gardens</LabelerName>
<SubstanceName>CALENDULA OFFICINALIS FLOWER; LACHESIS MUTA VENOM; GRAPHITE; ALLYLTHIOUREA</SubstanceName>
<StrengthNumber>10; 16; 10; 10</StrengthNumber>
<StrengthUnit>[hp_X]/28g; [hp_X]/28g; [hp_X]/28g; [hp_X]/28g</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2020-01-01</LastUpdate>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20191231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>10678-006-01</NDCCode>
<PackageDescription>566 L in 1 CYLINDER (10678-006-01)</PackageDescription>
<NDC11Code>10678-0006-01</NDC11Code>
<ProductNDC>10678-006</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Nitrous Oxide</ProprietaryName>
<NonProprietaryName>Nitrous Oxide</NonProprietaryName>
<DosageFormName>GAS</DosageFormName>
<RouteName>RESPIRATORY (INHALATION)</RouteName>
<StartMarketingDate>19470523</StartMarketingDate>
<MarketingCategoryName>UNAPPROVED MEDICAL GAS</MarketingCategoryName>
<LabelerName>Airgas-West, Inc.</LabelerName>
<SubstanceName>NITROUS OXIDE</SubstanceName>
<StrengthNumber>992</StrengthNumber>
<StrengthUnit>mL/L</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2019-09-21</LastUpdate>
<ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>10702-006-01</NDCCode>
<PackageDescription>100 TABLET, FILM COATED in 1 BOTTLE (10702-006-01) </PackageDescription>
<NDC11Code>10702-0006-01</NDC11Code>
<ProductNDC>10702-006</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Cyclobenzaprine Hydrochloride</ProprietaryName>
<NonProprietaryName>Cyclobenzaprine Hydrochloride</NonProprietaryName>
<DosageFormName>TABLET, FILM COATED</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20140731</StartMarketingDate>
<MarketingCategoryName>ANDA</MarketingCategoryName>
<ApplicationNumber>ANDA078048</ApplicationNumber>
<LabelerName>KVK-TECH, Inc.</LabelerName>
<SubstanceName>CYCLOBENZAPRINE HYDROCHLORIDE</SubstanceName>
<StrengthNumber>5</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Pharm_Classes>Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]</Pharm_Classes>
<Status>Active</Status>
<LastUpdate>2018-12-28</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20140731</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>Cyclobenzaprine hydrochloride tablets, USP is indicated as an adjunct to rest and physical therapy for relief of muscle spasm associated with acute, painful musculoskeletal conditions. Improvement is manifested by relief of muscle spasm and its associated signs and symptoms, namely, pain, tenderness, limitation of motion, and restriction in activities of daily living. Cyclobenzaprine hydrochloride tablets, USP should be used only for short periods (up to two or three weeks) because adequate evidence of effectiveness for more prolonged use is not available and because muscle spasm associated with acute, painful musculoskeletal conditions is generally of short duration and specific therapy for longer periods is seldom warranted. Cyclobenzaprine hydrochloride tablets, USP have not been found effective in the treatment of spasticity associated with cerebral or spinal cord disease, or in children with cerebral palsy.</IndicationAndUsage>
<Description>Cyclobenzaprine hydrochloride is a white, crystalline tricyclic amine salt with the empirical formula C 20H 21N HCl and a molecular weight of 311.9. It has a melting point of 217°C and a pKa of 8.47 at 25°C. It is freely soluble in water and alcohol, sparingly soluble in isopropanol, and insoluble in hydrocarbon solvents. If aqueous solutions are made alkaline, the free base separates. Cyclobenzaprine hydrochloride is designated chemically as 3-(5H-dibenzo [a,d] cyclohepten-5-ylidene)-N,N-dimethyl-1-propanamine hydrochloride, and has the following structural formula. Each 5 mg Cyclobenzaprine hydrochloride tablet for oral administration contains 5 mg Cyclobenzaprine hydrochloride. Each 10 mg Cyclobenzaprine hydrochloride tablet for oral administration contains 10 mg Cyclobenzaprine hydrochloride. Each tablet contains the following inactive ingredients: lactose monohydrate, microcrystalline cellulose, croscarmellose sodium, silicon dioxide, magnesium stearate, carnauba wax, titanium dioxide, polyethylene glycol, and iron oxide yellow. In addition, 5 mg tablets also contain polyvinyl alcohol, talc, lecithin, and FD&C yellow # 6 / sunset yellow FCF aluminum lake. In addition, 10 mg tablets also contain D&C yellow # 10 aluminum lake, FD&C yellow # 6 aluminum lake and hypromellose.</Description>
</NDC>
<NDC>
<NDCCode>10812-006-01</NDCCode>
<PackageDescription>1 TUBE in 1 CARTON (10812-006-01) > 50 mL in 1 TUBE</PackageDescription>
<NDC11Code>10812-0006-01</NDC11Code>
<ProductNDC>10812-006</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Neutrogena Healthy Defense Spf30</ProprietaryName>
<NonProprietaryName>Titanium Dioxide And Zinc Oxide</NonProprietaryName>
<DosageFormName>LOTION</DosageFormName>
<RouteName>TOPICAL</RouteName>
<StartMarketingDate>20091201</StartMarketingDate>
<EndMarketingDate>20150102</EndMarketingDate>
<MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
<ApplicationNumber>part352</ApplicationNumber>
<LabelerName>Neutrogena Corporation</LabelerName>
<SubstanceName>TITANIUM DIOXIDE; ZINC OXIDE</SubstanceName>
<StrengthNumber>50; 30</StrengthNumber>
<StrengthUnit>mg/mL; mg/mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2015-01-09</LastUpdate>
</NDC>
<NDC>
<NDCCode>11054-006-01</NDCCode>
<PackageDescription>85 L in 1 CYLINDER (11054-006-01) </PackageDescription>
<NDC11Code>11054-0006-01</NDC11Code>
<ProductNDC>11054-006</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Nitrogen, Refrigerated</ProprietaryName>
<NonProprietaryName>Nitrogen, Refrigerated</NonProprietaryName>
<DosageFormName>LIQUID</DosageFormName>
<RouteName>CUTANEOUS</RouteName>
<StartMarketingDate>19971106</StartMarketingDate>
<MarketingCategoryName>NDA</MarketingCategoryName>
<ApplicationNumber>NDA205839</ApplicationNumber>
<LabelerName>Airgas Usa, LLC</LabelerName>
<SubstanceName>NITROGEN</SubstanceName>
<StrengthNumber>992</StrengthNumber>
<StrengthUnit>mL/L</StrengthUnit>
<Status>Active</Status>
<LastUpdate>2026-06-16</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20271231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>19971106</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>11084-006-01</NDCCode>
<PackageDescription>47 mL in 1 BOTTLE, PLASTIC (11084-006-01) </PackageDescription>
<NDC11Code>11084-0006-01</NDC11Code>
<ProductNDC>11084-006</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Alcare Extra Hand Sanitizer</ProprietaryName>
<NonProprietaryName>Alcohol</NonProprietaryName>
<DosageFormName>SOLUTION</DosageFormName>
<RouteName>TOPICAL</RouteName>
<StartMarketingDate>20170301</StartMarketingDate>
<MarketingCategoryName>OTC MONOGRAPH DRUG</MarketingCategoryName>
<ApplicationNumber>505G(a)(3)</ApplicationNumber>
<LabelerName>SC Johnson Professional USA, Inc.</LabelerName>
<SubstanceName>ALCOHOL</SubstanceName>
<StrengthNumber>80</StrengthNumber>
<StrengthUnit>mL/100mL</StrengthUnit>
<Status>Active</Status>
<LastUpdate>2025-10-08</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20170301</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>for hand sanitizing to reduce bacteria on the skin.</IndicationAndUsage>
</NDC>
<NDC>
<NDCCode>11324-006-01</NDCCode>
<PackageDescription>8778 L in 1 CYLINDER (11324-006-01) </PackageDescription>
<NDC11Code>11324-0006-01</NDC11Code>
<ProductNDC>11324-006</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Air</ProprietaryName>
<NonProprietaryName>Air</NonProprietaryName>
<DosageFormName>GAS</DosageFormName>
<RouteName>RESPIRATORY (INHALATION)</RouteName>
<StartMarketingDate>20051001</StartMarketingDate>
<MarketingCategoryName>UNAPPROVED MEDICAL GAS</MarketingCategoryName>
<LabelerName>Linde Puerto Rico B.V.</LabelerName>
<SubstanceName>OXYGEN</SubstanceName>
<StrengthNumber>210</StrengthNumber>
<StrengthUnit>mL/L</StrengthUnit>
<Status>Active</Status>
<LastUpdate>2026-01-02</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>20051001</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>11559-006-01</NDCCode>
<PackageDescription>1 TUBE in 1 CARTON (11559-006-01) > 30 mL in 1 TUBE (11559-006-02)</PackageDescription>
<NDC11Code>11559-0006-01</NDC11Code>
<ProductNDC>11559-006</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Cyber White</ProprietaryName>
<ProprietaryNameSuffix>Brilliant Cells Full Spectrum Brightening Uv Protector Spf 50</ProprietaryNameSuffix>
<NonProprietaryName>Homosalate, Octisalate, Avobenzone, Oxybenzone</NonProprietaryName>
<DosageFormName>LOTION</DosageFormName>
<RouteName>TOPICAL</RouteName>
<StartMarketingDate>20100601</StartMarketingDate>
<MarketingCategoryName>OTC MONOGRAPH NOT FINAL</MarketingCategoryName>
<ApplicationNumber>part352</ApplicationNumber>
<LabelerName>ESTEE LAUDER INC</LabelerName>
<SubstanceName>HOMOSALATE; OCTISALATE; AVOBENZONE; OXYBENZONE</SubstanceName>
<StrengthNumber>5; 5; 3; 3</StrengthNumber>
<StrengthUnit>mL/100mL; mL/100mL; mL/100mL; mL/100mL</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2019-09-21</LastUpdate>
<ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20171231</ListingRecordCertifiedThrough>
</NDC>
<NDC>
<NDCCode>11673-006-01</NDCCode>
<PackageDescription>10 BLISTER PACK in 1 CARTON (11673-006-01) > 2 TABLET, FILM COATED in 1 BLISTER PACK</PackageDescription>
<NDC11Code>11673-0006-01</NDC11Code>
<ProductNDC>11673-006</ProductNDC>
<ProductTypeName>HUMAN OTC DRUG</ProductTypeName>
<ProprietaryName>Up And Up Fast Mucus Relief Severe Cold</ProprietaryName>
<NonProprietaryName>Acetaminophen, Dextromethorphan Hbr, Guaifenesin, Phenylephrine Hcl</NonProprietaryName>
<DosageFormName>TABLET, FILM COATED</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20150316</StartMarketingDate>
<EndMarketingDate>20211216</EndMarketingDate>
<MarketingCategoryName>OTC MONOGRAPH FINAL</MarketingCategoryName>
<ApplicationNumber>part341</ApplicationNumber>
<LabelerName>Target Corporation</LabelerName>
<SubstanceName>ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE</SubstanceName>
<StrengthNumber>325; 10; 200; 5</StrengthNumber>
<StrengthUnit>mg/1; mg/1; mg/1; mg/1</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2021-12-17</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<StartMarketingDatePackage>20150316</StartMarketingDatePackage>
<EndMarketingDatePackage>20211216</EndMarketingDatePackage>
<SamplePackage>N</SamplePackage>
</NDC>
<NDC>
<NDCCode>11994-006-02</NDCCode>
<PackageDescription>2 KIT in 1 PACKAGE, COMBINATION (11994-006-02) > 1 KIT in 1 KIT * 1 INJECTION in 1 VIAL (11994-002-01) * 1 mL in 1 VIAL (11994-004-01) </PackageDescription>
<NDC11Code>11994-0006-02</NDC11Code>
<ProductNDC>11994-006</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Neurolite</ProprietaryName>
<NonProprietaryName>Bicisate Dihydrochloride</NonProprietaryName>
<DosageFormName>KIT</DosageFormName>
<StartMarketingDate>19941123</StartMarketingDate>
<MarketingCategoryName>NDA</MarketingCategoryName>
<ApplicationNumber>NDA020256</ApplicationNumber>
<LabelerName>Lantheus Medical Imaging, Inc.</LabelerName>
<Status>Active</Status>
<LastUpdate>2022-11-29</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>19941123</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>Neurolite single photon emission computerized tomography (SPECT) is indicated as an adjunct to conventional CT or MRI imaging in the localization of stroke in patients in whom stroke has already been diagnosed. Neurolite is not indicated for assessment of functional viability of brain tissue. Also, Neurolite is not indicated for distinguishing between stroke and other brain lesions.</IndicationAndUsage>
<Description>This kit formulation consists of two nonradioactive vials: Vial A contains bicisate dihydrochloride (N, N'-1,2-ethylenediylbis-L-cysteine diethyl ester dihydrochloride) and a reducing agent as a lyophilized solid and vial B contains a buffer solution. Both vials are sterile and non-pyrogenic. The contents of vial A are lyophilized and stored under nitrogen. The pH of the solution before lyophilization is 2.7 ± 0.25. This vial is stored at 15-25°C. Protect from light. The contents of vial B are stored under air. The pH of the solution is 7.6 ± 0.4. This vial is stored at 15-25°C. This drug is administered by intravenous injection for diagnostic use after reconstitution with sterile, non-pyrogenic, oxidant-free Sodium Pertechnetate Tc99m Injection. The precise structure of the Technetium complex is [N, N'-ethylenedi-L-cysteinato(3-)]oxo[99mTc] technetium (V), diethyl ester.</Description>
</NDC>
<NDC>
<NDCCode>11994-006-05</NDCCode>
<PackageDescription>5 KIT in 1 PACKAGE, COMBINATION (11994-006-05) > 1 KIT in 1 KIT * 1 INJECTION in 1 VIAL (11994-002-01) * 1 mL in 1 VIAL (11994-004-01) </PackageDescription>
<NDC11Code>11994-0006-05</NDC11Code>
<ProductNDC>11994-006</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Neurolite</ProprietaryName>
<NonProprietaryName>Bicisate Dihydrochloride</NonProprietaryName>
<DosageFormName>KIT</DosageFormName>
<StartMarketingDate>19941123</StartMarketingDate>
<MarketingCategoryName>NDA</MarketingCategoryName>
<ApplicationNumber>NDA020256</ApplicationNumber>
<LabelerName>Lantheus Medical Imaging, Inc.</LabelerName>
<Status>Active</Status>
<LastUpdate>2022-11-29</LastUpdate>
<PackageNdcExcludeFlag>N</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>N</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20261231</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>19941123</StartMarketingDatePackage>
<SamplePackage>N</SamplePackage>
<IndicationAndUsage>Neurolite single photon emission computerized tomography (SPECT) is indicated as an adjunct to conventional CT or MRI imaging in the localization of stroke in patients in whom stroke has already been diagnosed. Neurolite is not indicated for assessment of functional viability of brain tissue. Also, Neurolite is not indicated for distinguishing between stroke and other brain lesions.</IndicationAndUsage>
<Description>This kit formulation consists of two nonradioactive vials: Vial A contains bicisate dihydrochloride (N, N'-1,2-ethylenediylbis-L-cysteine diethyl ester dihydrochloride) and a reducing agent as a lyophilized solid and vial B contains a buffer solution. Both vials are sterile and non-pyrogenic. The contents of vial A are lyophilized and stored under nitrogen. The pH of the solution before lyophilization is 2.7 ± 0.25. This vial is stored at 15-25°C. Protect from light. The contents of vial B are stored under air. The pH of the solution is 7.6 ± 0.4. This vial is stored at 15-25°C. This drug is administered by intravenous injection for diagnostic use after reconstitution with sterile, non-pyrogenic, oxidant-free Sodium Pertechnetate Tc99m Injection. The precise structure of the Technetium complex is [N, N'-ethylenedi-L-cysteinato(3-)]oxo[99mTc] technetium (V), diethyl ester.</Description>
</NDC>
<NDC>
<NDCCode>12121-006-01</NDCCode>
<PackageDescription>361 L in 1 CYLINDER (12121-006-01)</PackageDescription>
<NDC11Code>12121-0006-01</NDC11Code>
<ProductNDC>12121-006</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Nitrogen</ProprietaryName>
<NonProprietaryName>Nitrogen</NonProprietaryName>
<DosageFormName>GAS</DosageFormName>
<RouteName>RESPIRATORY (INHALATION)</RouteName>
<StartMarketingDate>19550101</StartMarketingDate>
<MarketingCategoryName>UNAPPROVED MEDICAL GAS</MarketingCategoryName>
<LabelerName>Badger Welding Supplies, Inc</LabelerName>
<SubstanceName>NITROGEN</SubstanceName>
<StrengthNumber>99</StrengthNumber>
<StrengthUnit>L/100L</StrengthUnit>
<Status>Deprecated</Status>
<LastUpdate>2014-11-14</LastUpdate>
</NDC>
<NDC>
<NDCCode>13107-006-01</NDCCode>
<PackageDescription>100 TABLET in 1 BOTTLE (13107-006-01)</PackageDescription>
<NDC11Code>13107-0006-01</NDC11Code>
<ProductNDC>13107-006</ProductNDC>
<ProductTypeName>HUMAN PRESCRIPTION DRUG</ProductTypeName>
<ProprietaryName>Citalopram</ProprietaryName>
<NonProprietaryName>Citalopram</NonProprietaryName>
<DosageFormName>TABLET</DosageFormName>
<RouteName>ORAL</RouteName>
<StartMarketingDate>20090101</StartMarketingDate>
<MarketingCategoryName>ANDA</MarketingCategoryName>
<ApplicationNumber>ANDA077031</ApplicationNumber>
<LabelerName>Aurolife Pharma LLC</LabelerName>
<SubstanceName>CITALOPRAM HYDROBROMIDE</SubstanceName>
<StrengthNumber>20</StrengthNumber>
<StrengthUnit>mg/1</StrengthUnit>
<Pharm_Classes>Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]</Pharm_Classes>
<Status>Deprecated</Status>
<LastUpdate>2019-09-21</LastUpdate>
<ProductNdcExcludeFlag>E</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>20181231</ListingRecordCertifiedThrough>
<IndicationAndUsage>A major depressive episode (DSM-IV) implies a prominent and relatively persistent (nearly every day for at least 2 weeks) depressed or dysphoric mood that usually interferes with daily functioning, and includes at least five of the following nine symptoms: depressed mood, loss of interest in usual activities, significant change in weight and/or appetite, insomnia or hypersomnia, psychomotor agitation or retardation, increased fatigue, feelings of guilt or worthlessness, slowed thinking or impaired concentration, a suicide attempt or suicidal ideation. The antidepressant action of citalopram tablets, USP in hospitalized depressed patients has not been adequately studied.</IndicationAndUsage>
<Description>Citalopram hydrobromide USP occurs as a fine, white to off-white powder. Citalopram hydrobromide is sparingly soluble in water and soluble in ethanol.</Description>
</NDC>
</NDCList>