Menopause
FDA Label NDC 61657-0527

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by White Manufacturing Inc. Dba Micro-west for the product Menopause (NDC 61657-0527). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredients, purpose, keep out of reach of children, indications, warning, directions, inactive ingredients, manufacture, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

CIMICIFUGA RACEMOSA [HPUS] 3X

SEPIA [HPUS] 12X

PULSATILLA [HPUS] 12X

USTILAGO MAIDIS [HPUS] 12X

SULFUR 12X
LACHESIS MUTUS [HPUS)  12X
BELLADONNA [HPUS 12X
SANGUINARIA 12X

Purpose

FOR THE TEMPORARY RELIEF OF HOT FLASHES, IRRITABILITY, NIGHT SWEATS, AND ABNORMAL MENSTRUAL FLOW DUE TO MENOPAUSE

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Indications

INDICATIONS: FOR THE TEMPORARY RELIEF OF HOT FLASHES, IRRITABILITY, NIGHT SWEATS, AND ABNORMAL MENSTRUAL FLOW DUE TO MENOPAUSE

Warning

WARNING: IF PREGNANT OR NURSING, PLEASE CONSULT YOUR PHYSICIAN BEFORE USING THIS PRODUCT

Directions

DIRECTIONS: ORALLY 6 DROPS, 4 TIMES A DAY

Inactive Ingredients

NOT MORE THAN 20% ALCOHOL

Manufacture

MANUFACTURED FOR MICRO-WEST

DOUGLAS, WY 82633

1-307-358-5066

Label

Image Of Bottle Label (Menopause)

Image Of Bottle Label (Menopause)

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