Menopause Relief

Product NDC

43742-0824

11-digit product format

437420824

Labeler code

43742

Product ID

43742-0824_95c00d8d-0f42-42c9-89ff-4d015d141521

Type

HUMAN OTC DRUG

Nonproprietary name

Sanguinaria Canadensis, Ignatia Amara, Sepia, Adenosinum Triphosphoricum Dinatrum, Bryonia (Alba), Cedron, DIM (3,3-Diindolymethane), Equol, Sulphur, Apiolum, Lachesis Mutus, Stannum Metallicum, Faecalis (Alkaligenes)

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2016-07-26

Marketing end

2023-06-28

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