1. Home
  2. Labeler Index
  3. Homeocare Laboratories
  4. NDC Product Code: 61727-314 Vigofem For Women

NDC 61727-314 Vigofem For Women

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 61727-314?
  5. Vigofem For Women Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
61727-314
Proprietary Name:
Vigofem For Women
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Homeocare Laboratories
Labeler Code:
61727
Product Label ID:
1ca16d37-53e7-4264-a693-15da8f94af64
Start Marketing Date: [9]
07-24-2012
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
10 MM
Score:
2

Code Structure Chart

Product Details

What is NDC 61727-314?

The NDC code 61727-314 is assigned by the FDA to the product Vigofem For Women which is product labeled by Homeocare Laboratories. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61727-314-90 90 tablet in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Vigofem For Women?

Chew one tablet slightly and allow to dissolve in the mouth, 3 times a day; or as directed by a physician. For best results take in a clean mouth, at least 15 mn. apart from food.

Which are Vigofem For Women UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Vigofem For Women Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".