NDC 72042-003 Burn Relief

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:
72042-003
Proprietary Name:
Burn Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Humn Pharmaceuticals Inc
Labeler Code:
72042
Start Marketing Date: [9]
05-16-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 72042-003-03

Package Description: 1 TUBE in 1 CARTON / 28300 mg in 1 TUBE

Product Details

What is NDC 72042-003?

The NDC code 72042-003 is assigned by the FDA to the product Burn Relief which is product labeled by Humn Pharmaceuticals Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72042-003-03 1 tube in 1 carton / 28300 mg 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 Burn Relief?

UsesTemporary relief of pain associated with:▪ minor burns ▪ minor skin irritationsTemporary protection of minor skin irritations

Which are Burn Relief UNII Codes?

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

Which are Burn Relief 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 Burn Relief?

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: 2045344 - allantoin 1.5 % / lidocaine HCl 4 % / menthol 1 % Topical Cream
  • RxCUI: 2045344 - allantoin 15 MG/ML / lidocaine hydrochloride 40 MG/ML / menthol 10 MG/ML 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".