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  4. NDC Product Code: 60986-1024 Female Tonic

NDC 60986-1024 Female Tonic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 60986-1024?
  4. Female Tonic Uses
  5. Active Ingredients UNII Codes
  6. 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:
60986-1024
Proprietary Name:
Female Tonic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Marco Pharma International Llc.
Labeler Code:
60986
Product Label ID:
ab3ba68a-85fd-4f65-84f3-73852985ac6f
Start Marketing Date: [9]
03-01-1992
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 60986-1024-7

Package Description: 236 mL in 1 BOTTLE, GLASS

Product Details

What is NDC 60986-1024?

The NDC code 60986-1024 is assigned by the FDA to the product Female Tonic which is product labeled by Marco Pharma International Llc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60986-1024-7 236 ml in 1 bottle, glass . 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 Female Tonic?

This product is used as For fatigue, mental and physical exhaustion, PMS, depression and irritability.

Which are Female Tonic UNII Codes?

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

Which are Female Tonic 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:

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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".