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  4. NDC Product Code: 52124-4016 Genuine First Aid Industrial First Aid

NDC 52124-4016 Genuine First Aid Industrial First Aid

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52124-4016?
  5. Genuine First Aid Industrial First Aid Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. 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:
52124-4016
Proprietary Name:
Genuine First Aid Industrial First Aid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Genuine First Aid, Llc
Labeler Code:
52124
Product Label ID:
a44e5837-62b5-4668-96fd-5aba8346925d
Start Marketing Date: [9]
05-03-2011
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
Shape:
ROUND (C48348)
Size(s):
10 MM
11 MM
Imprint(s):
44;352
AZ;234
44;157;ASPIRIN
Score:
1

Code Structure Chart

Product Details

What is NDC 52124-4016?

The NDC code 52124-4016 is assigned by the FDA to the product Genuine First Aid Industrial First Aid which is product labeled by Genuine First Aid, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52124-4016-6 1 kit in 1 kit * 2 tablet in 1 package (52124-0011-1) * 2 tablet in 1 package (52124-0010-1) * 2 tablet in 1 packet (52124-0009-1) * .5 g in 1 tube (52124-0003-1) * .9 g in 1 packet (52124-0004-1) * .8 ml in 1 package (52124-0001-1). 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 Industrial First Aid?

Tear open packet, unfold towelette and use to cleanse desired skin area.  Discard towelette appropriately after single use. Directions: clean affected area;  apply small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily; may be covered with a sterile bandage 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 do not use more than directed; the smallest effective dose should be used; do not take longer than 10 days, unless directed by a doctor.Adults and Children (12 years and older):  Take 1 tablet every 4 to 6 hours while symptoms persist.  If pain or fever does not respond to 1 tablet, 2 tablets may be used.  Do not exceed 6 tablets in 24 hours, unless directed by a doctor.Children under 12 years: Do not give to children under 12 years of age. do not use more than directedthe smallest effective dose should be useddrink a full glass of water with each dosedo not take longer than 10 days, unless directed by a doctor

Which are Genuine First Aid Industrial First Aid UNII Codes?

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

Which are Genuine First Aid Industrial First Aid 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 Industrial First Aid?

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: 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

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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".