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  4. NDC Product Code: 47046-154 Triple Antibiotic First Aid Antibiotic

NDC 47046-154 Triple Antibiotic First Aid Antibiotic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 47046-154?
  4. Triple Antibiotic First Aid Antibiotic 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:
47046-154
Proprietary Name:
Triple Antibiotic First Aid Antibiotic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Anicare Pharmaceuticals Pvt. Ltd
Labeler Code:
47046
Product Label ID:
b659d3cf-97c4-5ca2-e053-2a95a90a9371
Start Marketing Date: [9]
12-09-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 47046-154-02

Package Description: 1 TUBE in 1 BOX / 14 g in 1 TUBE (47046-154-01)

Product Details

What is NDC 47046-154?

The NDC code 47046-154 is assigned by the FDA to the product Triple Antibiotic First Aid Antibiotic which is product labeled by Anicare Pharmaceuticals Pvt. Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 47046-154-02 1 tube in 1 box / 14 g in 1 tube (47046-154-01). 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 Triple Antibiotic First Aid Antibiotic?

Usesfirst aid to help prevent infection inminor cutsscrapesburns

Which are Triple Antibiotic First Aid Antibiotic UNII Codes?

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

Which are Triple Antibiotic First Aid Antibiotic 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 Triple Antibiotic First Aid Antibiotic?

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: 204602 - bacitracin 400 UNT / neomycin 3.5 MG / polymyxin B 5000 UNT per GM Topical Ointment
  • RxCUI: 204602 - bacitracin 0.4 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical Ointment
  • RxCUI: 204602 - bacitracin 400 UNT / neomycin 3.5 MG (as neomycin sulfate 5 MG) / polymyxin B 5000 UNT per GM Topical Ointment

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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".