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  4. NDC Product Code: 70146-003 Womens Sports Balm

NDC 70146-003 Womens Sports Balm

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70146-003?
  4. Womens Sports Balm 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 certification is expired.
NDC Product Code:
70146-003
Proprietary Name:
Womens Sports Balm
Product Type: [3]
EXPIRED PRODUCT and EXCLUDED from the NDC Directory
Labeler Name: [5]
Dr.sankunni's Ayurvedic Research Foundation Private Limited
Labeler Code:
70146
Product Label ID:
928e421d-2a62-463a-a5ad-ce412654dc8f
Start Marketing Date: [9]
10-15-2015
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
E
Code Structure:
Code Navigator:

Product Packages

NDC Code 70146-003-00

Package Description: 20 g in 1 JAR

NDC Code 70146-003-01

Package Description: 5 g in 1 JAR

Product Details

What is NDC 70146-003?

The NDC code 70146-003 is assigned by the FDA to the product Womens Sports Balm which is product labeled by Dr.sankunni's Ayurvedic Research Foundation Private Limited. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 70146-003-00 20 g in 1 jar , 70146-003-01 5 g in 1 jar . 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 Womens Sports Balm?

ZENfor aches & painswomen's sports balm lavender oilideal for:aches & pains related tosports injuriesminor arthritissore musclesleg crampscrampsstrains and sprains

Which are Womens Sports Balm UNII Codes?

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

Which are Womens Sports Balm 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".