NDC 59779-621 Cvs Medicated Anti-itch

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:
59779-621
Proprietary Name:
Cvs Medicated Anti-itch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs Pharmacy
Labeler Code:
59779
Start Marketing Date: [9]
07-08-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 59779-621-64

Package Description: 1 TUBE in 1 CARTON / 56 g in 1 TUBE

Product Details

What is NDC 59779-621?

The NDC code 59779-621 is assigned by the FDA to the product Cvs Medicated Anti-itch which is product labeled by Cvs Pharmacy. The product's dosage form is . The product is distributed in a single package with assigned NDC code 59779-621-64 1 tube in 1 carton / 56 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 Cvs Medicated Anti-itch?

UsesFor the temporary relief of pain and discomfort cause by - minor burns - sunburn - scrapes - insect bites - minor skin irritations - rashes due to poison ivy, oak and sumac

Which are Cvs Medicated Anti-itch UNII Codes?

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

Which are Cvs Medicated Anti-itch 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 Cvs Medicated Anti-itch?

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: 1116155 - menthol 1 % / pramoxine HCl 1 % Topical Cream
  • RxCUI: 1116155 - menthol 10 MG/ML / pramoxine hydrochloride 10 MG/ML Topical Cream
  • RxCUI: 1116155 - menthol 1 % / pramoxine hydrochloride 1 % 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".