MENOPAUSE RELIEF
- Product NDC
- 43742-0566
- 11-digit product format
- 437420566
- Labeler code
- 43742
- Product ID
- 43742-0566_8f425ee7-663a-4f1d-a95c-ef18e48178ae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sanguinaria Canadensis, Ignatia Amara, Sepia, Adenosinum Triphosphoricum Disodium, Bryonia (Alba), Cedron, DIM (Diindolylmethane), Equol, Sulphur, Apiolum, Lachesis Mutus, Stannum Metallicum, Faecalis (Alkaligenes)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2015-02-19
- Marketing end
- 2020-12-10
- Substance
- SANGUINARIA CANADENSIS ROOT; STRYCHNOS IGNATII SEED; SEPIA OFFICINALIS JUICE; ADENOSINE TRIPHOSPHATE DISODIUM; BRYONIA ALBA ROOT; SIMABA CEDRON SEED; 3,3'-DIINDOLYLMETHANE; 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_X]/mL; [hp_C]/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record