Label: HCG DETOX (human chorionic gonadotropin- hcg, liquid
- NDC Code(s): 57520-0387-1
- Packager: Apotheca Company
- 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.
Updated December 10, 2010
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- ACTIVE INGREDIENT
WARNINGS: If pregnant or breast-feeding, do not use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
If conditions worsen, recur or persist for more than 7 days, consult your physician.
Do not use if tamper evident seal is broken or missing.
- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- PRINCIPAL DISPLAY PANEL
INGREDIENTS AND APPEARANCE
human chorionic gonadotropin (hcg), liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57520-0387 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HUMAN CHORIONIC GONADOTROPIN (UNII: 20ED16GHEB) (HUMAN CHORIONIC GONADOTROPIN - UNII:20ED16GHEB) HUMAN CHORIONIC GONADOTROPIN 60 [hp_X] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57520-0387-1 60 mL in 1 BOTTLE, DROPPER Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 12/10/2010 Labeler - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture