Label: GULF DETOX 6038- gulf detox liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 63083-6038-2 - Packager: Professional Complementary Health Formulas
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated August 15, 2019
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INGREDIENTS AND APPEARANCE
GULF DETOX 6038
gulf detox liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63083-6038 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ARCTIUM LAPPA ROOT OIL (UNII: 55DGS3F5YG) (ARCTIUM LAPPA ROOT OIL - UNII:55DGS3F5YG) ARCTIUM LAPPA ROOT OIL 3 [hp_X] in 59 mL TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375) TARAXACUM OFFICINALE 3 [hp_X] in 59 mL TRIFOLIUM PRATENSE FLOWER (UNII: 4JS0838828) (TRIFOLIUM PRATENSE FLOWER - UNII:4JS0838828) TRIFOLIUM PRATENSE FLOWER 3 [hp_X] in 59 mL CHLOROPHYLL (UNII: 00WNZ48OR9) (CHLOROPHYLL - UNII:00WNZ48OR9) CHLOROPHYLL 6 [hp_X] in 59 mL ANTHRACENE (UNII: EH46A1TLD7) (ANTHRACENE - UNII:EH46A1TLD7) ANTHRACENE 30 [hp_X] in 59 mL BENZENE (UNII: J64922108F) (BENZENE - UNII:J64922108F) BENZENE 30 [hp_X] in 59 mL XYLENE (MIXED ISOMERS) (UNII: D856J1047R) (XYLENE (MIXED ISOMERS) - UNII:D856J1047R) XYLENE (MIXED ISOMERS) 30 [hp_X] in 59 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL 12 [hp_X] in 59 mL LIQUID PETROLEUM (UNII: 6ZAE7X688J) (LIQUID PETROLEUM - UNII:6ZAE7X688J) LIQUID PETROLEUM 12 [hp_X] in 59 mL POLYCYCLIC AROMATIC HYDROCARBONS (UNII: 0TNN3Q0D4D) (POLYCYCLIC AROMATIC HYDROCARBONS - UNII:0TNN3Q0D4D) POLYCYCLIC AROMATIC HYDROCARBONS 30 [hp_X] in 59 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63083-6038-2 59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/15/1985 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/15/1984 Labeler - Professional Complementary Health Formulas (167339027) Registrant - Natural Pharmaceutical Manufacturing LLC (015624923) Establishment Name Address ID/FEI Business Operations Natural Pharmaceutical Manufacturing LLC 015624923 manufacture(63083-6038)