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  4. NDC Product Code: 52124-0003 Genuine Triple Antibiotic

NDC 52124-0003 Genuine Triple Antibiotic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52124-0003?
  4. Genuine Triple 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:
52124-0003
Proprietary Name:
Genuine Triple Antibiotic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Genuine First Aid Llc
Labeler Code:
52124
Product Label ID:
4ad9d0a5-cd17-0808-e054-00144ff8d46c
Start Marketing Date: [9]
02-16-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 52124-0003-1

Package Description: .5 g in 1 TUBE

NDC Code 52124-0003-2

Package Description: 10 PACKET in 1 BOX / .5 g in 1 PACKET

NDC Code 52124-0003-3

Package Description: 100 PACKET in 1 CARTON / .5 g in 1 PACKET

Product Details

What is NDC 52124-0003?

The NDC code 52124-0003 is assigned by the FDA to the product Genuine Triple Antibiotic which is product labeled by Genuine First Aid Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 52124-0003-1 .5 g in 1 tube , 52124-0003-2 10 packet in 1 box / .5 g in 1 packet, 52124-0003-3 100 packet in 1 carton / .5 g in 1 packet. 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 Genuine Triple Antibiotic?

For External use only.Keep out of Reach of Children.Stop use if unusual redness, swelling or other symptoms occur, consult a physician immediately.Do not uses in eyes or over large areas of the body.Tear open packet, unfold towelette and use to cleanse desired skin area. Discard towelette appropriately after single use.

Which are Genuine Triple Antibiotic UNII Codes?

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

Which are Genuine Triple 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 Genuine Triple 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: 1046313 - benzocaine 6 % / ethanol 60 % Medicated Pad
  • RxCUI: 1046313 - benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated Pad
  • RxCUI: 1046313 - benzocaine 6 % / ethanol 60 % Topical Swab
  • 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

* 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".