1. Home
  2. Labeler Index
  3. Rite Aid
  4. NDC Product Code: 11822-7799 Medicated Pain Relief Foot Cvs

NDC 11822-7799 Medicated Pain Relief Foot Cvs

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 11822-7799?
  4. Medicated Pain Relief Foot Cvs 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:
11822-7799
Proprietary Name:
Medicated Pain Relief Foot Cvs
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rite Aid
Labeler Code:
11822
Product Label ID:
0fc56798-4879-4969-bfc3-1ded46f704be
Start Marketing Date: [9]
03-08-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 11822-7799-4

Package Description: 133 mL in 1 CAN

Product Details

What is NDC 11822-7799?

The NDC code 11822-7799 is assigned by the FDA to the product Medicated Pain Relief Foot Cvs which is product labeled by Rite Aid. The product's dosage form is . The product is distributed in a single package with assigned NDC code 11822-7799-4 133 ml in 1 can . 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 Medicated Pain Relief Foot Cvs?

 Temporarily relieves pain and itching due to: • sunburn • minor burns • minor cuts • scrapes • insect bites • minor skin irritations

Which are Medicated Pain Relief Foot Cvs UNII Codes?

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

Which are Medicated Pain Relief Foot Cvs 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 Medicated Pain Relief Foot Cvs?

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:

* 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".