NDC 51852-100 First Aid Triple Antibiotic And Pain Relief Maximum Strength

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:
51852-100
Proprietary Name:
First Aid Triple Antibiotic And Pain Relief Maximum Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Lifelabs, A Division Of Atico International Usa, Inc.
Labeler Code:
51852
Start Marketing Date: [9]
11-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Product Packages

NDC Code 51852-100-01

Package Description: 1 TUBE in 1 CARTON / 28 g in 1 TUBE

Product Details

What is NDC 51852-100?

The NDC code 51852-100 is assigned by the FDA to the product First Aid Triple Antibiotic And Pain Relief Maximum Strength which is product labeled by Lifelabs, A Division Of Atico International Usa, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51852-100-01 1 tube in 1 carton / 28 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 First Aid Triple Antibiotic And Pain Relief Maximum Strength?

UsesFirst aid to help prevent infection in minor cuts, scrapes, and burnsFirst aid for the temporary relief of pain in minor cuts, scrapes, and burns

Which are First Aid Triple Antibiotic And Pain Relief Maximum Strength UNII Codes?

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

Which are First Aid Triple Antibiotic And Pain Relief Maximum Strength 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 First Aid Triple Antibiotic And Pain Relief Maximum Strength?

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: 1359350 - bacitracin 500 UNT / neomycin 3.5 MG / polymyxin B 10,000 UNT / pramoxine HCl 10 MG per GM Topical Ointment
  • RxCUI: 1359350 - bacitracin 0.5 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 10 UNT/MG / pramoxine hydrochloride 0.01 MG/MG 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".