Label: DHEA (dhea- dehydroepiandrosterone liquid
- NDC Code(s): 43742-0564-1
- Packager: Deseret Biologicals, Inc.
- 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 September 23, 2024
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- ACTIVE INGREDIENT:
- PURPOSE:
- USES:
- WARNINGS:
- KEEP OUT OF REACH OF CHILDREN:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
DHEA
dhea (dehydroepiandrosterone) liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0564 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PRASTERONE (UNII: 459AG36T1B) (PRASTERONE - UNII:459AG36T1B) PRASTERONE 6 [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:43742-0564-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 01/19/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 01/19/2015 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-0564) , api manufacture(43742-0564) , label(43742-0564) , pack(43742-0564)