NDC 61657-0971 Total Fem-bal

NDC Product Code 61657-0971

NDC 61657-0971-1

Package Description: 30 mL in 1 BOTTLE, PUMP

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Total Fem-bal with NDC 61657-0971 is a product labeled by White Manufacturing Inc. Dba Micro West. The generic name of Total Fem-bal is . The product's dosage form is and is administered via form.

Labeler Name: White Manufacturing Inc. Dba Micro West

Dosage Form: -

Product Type: What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: White Manufacturing Inc. Dba Micro West
Labeler Code: 61657
Start Marketing Date: 04-02-2007 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2018 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: I What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Total Fem-bal Product Label Images

Total Fem-bal Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

EACH MULTI POTENCIES OF 12X, 30X, LM1ADRENALINUM CHOLESTERINUMFOLLICULINUMHYPOTHALAMUSOOPHORINUMPULSATILLA

Directions

TAKE 2 PUMP SPRAYS 3 TIMES A DAILY.  HOLD UNDER TONGUE FOR 30 SECONDS BEFORE SWALLOWING. MORE FREQUENT DOSAGES MAY BE USED ACCORDING TO SYMPTOMATIC NEEDS. FOR AGES 12 TO ADULT

Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Warning

WARNING: WARNINGS: STOP USE AND CALL A DOCTOR if symptoms persist or worsen. CONTAINS ALCOHOL: in case of accidental overdose, consult a poison control center immediatelyOTHER INFORMATION: Tamper resistant for your protection. Use only if safety seal is intact

Pregnancy

IF PREGNANT OR BREAST FEEDING, consult a healthcare professional before use

Purpose

FOR HORMONAL IMBALANCES ASSOCIATED WITH PREMENSTRUAL SYNDROME, IRREGULAR MENSTRUAL CYCLE, WATER RETENTION, DEPRESSION, IRRITABILITY AND MOODINESS

Inactive Ingredients

POTASSIUM SORBATE, CITRIC ACID, PURIFIED WATER

Indications

INDICATIONS: FORTHE TEMPORARY RELIEF OF  HORMONAL IMBALANCES ASSOCIATED WITH PREMENSTRUAL SYNDROME, IRREGULAR MENSTRUAL CYCLE, WATER RETENTION, DEPRESSION, IRRITABILITY AND MOODINESS

Manufacture

MANUFACTURED FOR MICRO-WESTP.O. Box 950DOUGLAS, WY 826331-307-358-5066

* Please review the disclaimer below.