NDC 76347-120 Foot Rehab Pain Relief And Moisturizer Mission

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76347-120
Proprietary Name:
Foot Rehab Pain Relief And Moisturizer Mission
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Mission Product Holdings
Labeler Code:
76347
Start Marketing Date: [9]
11-05-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 76347-120-01

Package Description: 85 g in 1 TUBE

Product Details

What is NDC 76347-120?

The NDC code 76347-120 is assigned by the FDA to the product Foot Rehab Pain Relief And Moisturizer Mission which is product labeled by Mission Product Holdings. The product's dosage form is . The product is distributed in a single package with assigned NDC code 76347-120-01 85 g in 1 tube . 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 Foot Rehab Pain Relief And Moisturizer Mission?

Stop use and ask a doctor if- condition worsens or symptoms persist for more than 7 days- Symptoms clear up and occur again within a few days.- excessive skin irritation occurs

Which are Foot Rehab Pain Relief And Moisturizer Mission UNII Codes?

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

Which are Foot Rehab Pain Relief And Moisturizer Mission 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 Foot Rehab Pain Relief And Moisturizer Mission?

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:
  • RxCUI: 1358722 - Foot Rehab Pain & Moisture (menthol 10 % MG/ML / methyl salicylate 15 % ) Topical Cream
  • RxCUI: 1358722 - menthol 100 MG/ML / methyl salicylate 150 MG/ML Topical Cream [Foot Rehab Pain & Moisture]
  • RxCUI: 311498 - menthol 10 % / methyl salicylate 15 % Topical Cream
  • RxCUI: 311498 - menthol 100 MG/ML / methyl salicylate 150 MG/ML Topical Cream
  • RxCUI: 311498 - menthol 10 GM / methyl salicylate 15 GM per 100 GM Topical Cream

* 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".