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NDC 15127-721 Select Brand Anti-itch

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 15127-721?
  4. Select Brand Anti-itch 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:
15127-721
Proprietary Name:
Select Brand Anti-itch
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Select Brand
Labeler Code:
15127
Product Label ID:
0bacd190-b118-0df3-e054-00144ff8d46c
Start Marketing Date: [9]
10-03-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 15127-721-01

Package Description: 1 TUBE in 1 CARTON / 28.3 g in 1 TUBE

Product Details

What is NDC 15127-721?

The NDC code 15127-721 is assigned by the FDA to the product Select Brand Anti-itch which is product labeled by Select Brand. The product's dosage form is . The product is distributed in a single package with assigned NDC code 15127-721-01 1 tube in 1 carton / 28.3 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 Select Brand Anti-itch?

Adults and children 2 years and older: apply to affected area not more than 3 or 4 times dailychildren under 2 years: consult a doctor

Which are Select Brand Anti-itch UNII Codes?

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

Which are Select Brand 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 Select Brand 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".