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  4. NDC Product Code: 51141-0238 Atopalm First Aid Triple Antibiotic Protection Moisturizing And Pain Relief

NDC 51141-0238 Atopalm First Aid Triple Antibiotic Protection Moisturizing And Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 51141-0238?
  4. Atopalm First Aid Triple Antibiotic Protection Moisturizing And Pain Relief 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:
51141-0238
Proprietary Name:
Atopalm First Aid Triple Antibiotic Protection Moisturizing And Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Neopharm Co., Ltd.
Labeler Code:
51141
Product Label ID:
deaa865f-ec8f-42eb-ac34-fde9985f1391
Start Marketing Date: [9]
08-08-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 51141-0238?

The NDC code 51141-0238 is assigned by the FDA to the product Atopalm First Aid Triple Antibiotic Protection Moisturizing And Pain Relief which is product labeled by Neopharm Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51141-0238-1 1 tube in 1 carton / 28.3 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 Atopalm First Aid Triple Antibiotic Protection Moisturizing And Pain Relief?

Adults and children 2 years of age and olderclean the affected area and dry throughlyapply a small amount (equal to the surface area of the tip of a finger) on the area 1 to 3 times dailymay be covered with a sterile bandageChildren under 2 yrs. of ageConsult a doctor.

Which are Atopalm First Aid Triple Antibiotic Protection Moisturizing And Pain Relief UNII Codes?

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

Which are Atopalm First Aid Triple Antibiotic Protection Moisturizing And Pain 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 Atopalm First Aid Triple Antibiotic Protection Moisturizing And Pain 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: 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
  • RxCUI: 1359352 - ATOPALM First Aid and Pain Relief 500 UNT / 3.5 MG / 10,000 UNT / 10 MG per GM Topical Ointment
  • RxCUI: 1359352 - bacitracin 0.5 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 10 UNT/MG / pramoxine hydrochloride 0.01 MG/MG Topical Ointment [Atopalm First Aid Moisturizing and Pain Relief]
  • RxCUI: 1359352 - Atopalm First Aid Moisturizing and Pain Relief (bacitracin 500 UNT / neomycin 3.5 MG / polymyxin B 10,000 UNT / pramoxine hydrochloride 10 MG) 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".