MENOPAUSE RELIEF
- Product NDC
- 43742-0556
- 11-digit product format
- 437420556
- Labeler code
- 43742
- Product ID
- 43742-0556_b95e766f-2e12-46db-adc0-74acc1b2c154
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sanguinaria Canadensis, Ignatia Amara, Sepia, Adenosinum Triphosphoricum Disodium, Bryonia (Alba), Cedron, Equol, Sulphur, Apiolum, Lachesis Mutus, Stannum Metallicum, Faecalis (Alkaligenes)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2014-12-09
- Marketing end
- 2020-01-20
- Substance
- SANGUINARIA CANADENSIS ROOT; STRYCHNOS IGNATII SEED; SEPIA OFFICINALIS JUICE; ADENOSINE TRIPHOSPHATE DISODIUM; BRYONIA ALBA ROOT; SIMABA CEDRON SEED; EQUOL, (+)-; SULFUR; APIOLE (PARSLEY); LACHESIS MUTA VENOM; TIN; ALCALIGENES FAECALIS
- Active strength
- 3 [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_X]/mL; [hp_X]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record