1. Home
  2. Labeler Index
  3. Taro Pharmaceuticals U.s.a., Inc.
  4. NDC Product Code: 51672-5308 Beerx Muscle And Joint Pain Relief

NDC 51672-5308 Beerx Muscle And Joint Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51672-5308?
  4. Beerx Muscle And Joint Pain Relief 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:
51672-5308
Proprietary Name:
Beerx Muscle And Joint Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Taro Pharmaceuticals U.s.a., Inc.
Labeler Code:
51672
Product Label ID:
2b8b2581-0be9-422c-b6f7-8f988e109378
Start Marketing Date: [9]
10-05-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 51672-5308?

The NDC code 51672-5308 is assigned by the FDA to the product Beerx Muscle And Joint Pain Relief which is product labeled by Taro Pharmaceuticals U.s.a., Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51672-5308-1 1 jar in 1 box / 30 ml 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 Beerx Muscle And Joint Pain Relief?

 Adults and children 18 years of age and older: ● use only as directed ● apply to affected area but no more than 3 to 4 times daily ● massage onto painful area until thoroughly absorbed ● wash hands with soap and water after applyingChildren under 18 years of age:consult a doctor

Which are Beerx Muscle And Joint Pain Relief UNII Codes?

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

Which are Beerx Muscle And Joint Pain Relief 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".