Hormone Combination
- Product NDC
- 43742-0582
- 11-digit product format
- 437420582
- Labeler code
- 43742
- Product ID
- 43742-0582_ad5c6df6-58e7-4013-96b3-6bc7c4a4d899
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Salsolinol Hydrochloride, Cholesterinum, DHEA (Dehydroepiandrosterone), 7-Keto-DHEA (Dehydroepiandrosterone), Folliculinum, Oophorinum (Suis), Progesterone, Testosterone, Cortisone Aceticum, Aldosterone, Androsterone, Follicle Stimulating Hormone
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-06-03
- Marketing end
- 2020-10-27
- Substance
- SALSOLINOL HYDROCHLORIDE, (+/-)-; CHOLESTEROL; PRASTERONE; 7-KETO-DEHYDROEPIANDROSTERONE; ESTRONE; SUS SCROFA OVARY; PROGESTERONE; TESTOSTERONE; CORTISONE ACETATE; ALDOSTERONE; ANDROSTERONE; FOLLITROPIN
- Active strength
- 6 [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_C]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record