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  4. NDC Product Code: 76168-331 Ultra Strength Pain Relief Balm Ultra Strength

NDC 76168-331 Ultra Strength Pain Relief Balm Ultra Strength

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 76168-331?
  4. Ultra Strength Pain Relief Balm Ultra Strength Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76168-331
Proprietary Name:
Ultra Strength Pain Relief Balm Ultra Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Velocity Pharma Llc
Labeler Code:
76168
Product Label ID:
5f791159-c388-4c77-8aca-35e4c3f7cacd
Start Marketing Date: [9]
09-10-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76168-331-18

Package Description: 1 JAR in 1 PACKAGE / 18 g in 1 JAR

Product Details

What is NDC 76168-331?

The NDC code 76168-331 is assigned by the FDA to the product Ultra Strength Pain Relief Balm Ultra Strength which is product labeled by Velocity Pharma Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76168-331-18 1 jar in 1 package / 18 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 Ultra Strength Pain Relief Balm Ultra Strength?

For adults and children over 12, rub well on the affected area. Repeat 3 to 4 times dailyFor children 12 years of age or younger, consult a doctor before use.

Which are Ultra Strength Pain Relief Balm Ultra Strength UNII Codes?

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

  • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
  • CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)

Which are Ultra Strength Pain Relief Balm Ultra Strength 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:

What is the NDC to RxNorm Crosswalk for Ultra Strength Pain Relief Balm Ultra Strength?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".