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  4. NDC Product Code: 52124-0004 Genuine First Aid Burn Antiseptic Pain Relief With Aloe

NDC 52124-0004 Genuine First Aid Burn Antiseptic Pain Relief With Aloe

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 52124-0004?
  4. Genuine First Aid Burn Antiseptic Pain Relief With Aloe 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.

Get all the details for National Drug Code (NDC) 52124-0004 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
52124-0004
Proprietary Name:
Genuine First Aid Burn Antiseptic Pain Relief With Aloe
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Genuine First Aid
Labeler Code:
52124
Product Label ID:
fee1f9cd-7234-4e02-afae-1386af6a4775
FDA Application Number: [6]
part333A
Marketing Category: [8]
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date: [9]
04-23-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 52124-0004?

The NDC code 52124-0004 is assigned by the FDA to the product Genuine First Aid Burn Antiseptic Pain Relief With Aloe which is product labeled by Genuine First Aid. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 52124-0004-1 .9 g in 1 packet , 52124-0004-2 6 packet in 1 box / .9 g in 1 packet, 52124-0004-3 100 packet in 1 carton / .9 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 First Aid Burn Antiseptic Pain Relief With Aloe?

Wipe Injection site vigorously and discard. Adults and children 2 years of age and olderclean affected area.apply a small amount of this product on the area 1 to 3 times daily.may be covered with a sterile bandagechildren under 2 years of age: consult a doctor Clean intended area thoroughly with pad. Discard after single use.

Which are Genuine First Aid Burn Antiseptic Pain Relief With Aloe UNII Codes?

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

Which are Genuine First Aid Burn Antiseptic Pain Relief With Aloe 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 First Aid Burn Antiseptic Pain Relief With Aloe?

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: 1012100 - benzalkonium chloride 0.13 % / lidocaine HCl 0.5 % Topical Cream
  • RxCUI: 1012100 - benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 5 MG/ML Topical Cream
  • RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical Cream
  • RxCUI: 1046313 - benzocaine 6 % / ethanol 60 % Medicated Pad
  • RxCUI: 1046313 - benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated Pad

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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.

[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".