Menopause Relief

Product NDC

43742-1311

11-digit product format

437421311

Labeler code

43742

Product ID

43742-1311_1a0da555-74bc-41c3-93ac-39abc32895c6

Type

HUMAN OTC DRUG

Nonproprietary name

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

Dosage form

LIQUID

Route

ORAL

Labeler

Deseret Biologicals, Inc.

Marketing category

UNAPPROVED HOMEOPATHIC

Marketing start

2018-08-28

Marketing end

2024-03-05

Substance

3,3'-DIINDOLYLMETHANE; ADENOSINE TRIPHOSPHATE DISODIUM; ALCALIGENES FAECALIS; APIOLE (PARSLEY); BRYONIA ALBA ROOT; EQUOL, (-)-; LACHESIS MUTA VENOM; SANGUINARIA CANADENSIS ROOT; SEPIA OFFICINALIS JUICE; SIMABA CEDRON SEED; STRYCHNOS IGNATII SEED; SULFUR; TIN

Active strength

6 [hp_X]/mL; [hp_X]/mL; [hp_C]/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

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record