Label: ESTROGEN- folliculinum, oophorinum, liquid
- NDC Code(s): 43742-0066-1
- 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 June 28, 2018
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- ACTIVE INGREDIENTS:
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HOMEOPATHIC INDICATIONS:
For temporary relief of symptoms related to breast tenderness, hot flashes, irregular periods, mood swings, headaches, lactose intolerance and allergies to dairy products including rash, hives, diarrhea, cramps, coughing, sneezing and runny nose.**
**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
- WARNINGS:
- DIRECTIONS:
- INACTIVE INGREDIENTS:
- KEEP OUT OF REACH OF CHILDREN:
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HOMEOPATHIC INDICATIONS:
For temporary relief of symptoms related to breast tenderness, hot flashes, irregular periods, mood swings, headaches, lactose intolerance and allergies to dairy products including rash, hives, diarrhea, cramps, coughing, sneezing and runny nose.**
**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.
- QUESTIONS:
- PACKAGE LABEL DISPLAY:
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INGREDIENTS AND APPEARANCE
ESTROGEN
folliculinum, oophorinum, liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-0066 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ESTRONE (UNII: 2DI9HA706A) (ESTRONE - UNII:2DI9HA706A) ESTRONE 8 [hp_X] in 1 mL SUS SCROFA OVARY (UNII: S7YTV04R8O) (SUS SCROFA OVARY - UNII:S7YTV04R8O) SUS SCROFA OVARY 8 [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:43742-0066-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 07/10/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/10/2012 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-0066) , api manufacture(43742-0066) , label(43742-0066) , pack(43742-0066)