NDC 11960-0049 Nitrotan

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:
11960-0049
Proprietary Name:
Nitrotan
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
11960
Start Marketing Date: [9]
07-15-1992
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 11960-0049?

The NDC code 11960-0049 is assigned by the FDA to the product Nitrotan which is product labeled by Cramer Products Inc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 11960-0049-1 113 g in 1 can , 11960-0049-2 226 g 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 Nitrotan?

Nitrotan is a highly effective germicide, formulated expressly for minor wounds and burns.  Its four-way action reduces pain, checks capillary bleeding, promotes healing, and aids in the prevention of infection.This product is used as . Purpose   AntisepticBacteriacideAstringentBacteriacide

Which are Nitrotan UNII Codes?

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

Which are Nitrotan 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 Nitrotan?

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: 1432138 - benzyl alcohol 6.1 % / isopropyl alcohol 62 % / picric acid 0.2 % / tannic acid 1.5 % Topical Spray
  • RxCUI: 1432138 - benzyl alcohol 0.061 ML/ML / isopropyl alcohol 0.62 ML/ML / picric acid 2 MG/ML / tannic acid 15 MG/ML Topical Spray
  • RxCUI: 1432143 - Nitrotan 62 % / 6.1 % / 1.5 % / 0.2 % Topical Spray
  • RxCUI: 1432143 - benzyl alcohol 0.061 ML/ML / isopropyl alcohol 0.62 ML/ML / picric acid 2 MG/ML / tannic acid 15 MG/ML Topical Spray [Nitrotan]
  • RxCUI: 1432143 - Nitrotan (benzyl alcohol 6.1 % / isopropyl alcohol 62 % / picric acid 0.2 % / tannic acid 1.5 % ) Topical Spray

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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".