NDC 0924-5701 First Aid And Burn

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:
0924-5701
Proprietary Name:
First Aid And Burn
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Acme United Corporation
Labeler Code:
0924
Start Marketing Date: [9]
01-27-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 0924-5701-02

Package Description: 6 PACKET in 1 BAG / .9 g in 1 PACKET (0924-5701-01)

NDC Code 0924-5701-03

Package Description: 6 PACKET in 1 BAG / .9 g in 1 PACKET (0924-5701-01)

NDC Code 0924-5701-04

Package Description: 10 PACKET in 1 BOX / .9 g in 1 PACKET (0924-5701-01)

NDC Code 0924-5701-05

Package Description: 12 PACKET in 1 BOX / .9 g in 1 PACKET (0924-5701-01)

NDC Code 0924-5701-06

Package Description: 25 PACKET in 1 BOX / .9 g in 1 PACKET (0924-5701-01)

NDC Code 0924-5701-07

Package Description: 60 PACKET in 1 BOX / .9 g in 1 PACKET (0924-5701-01)

NDC Code 0924-5701-08

Package Description: 144 PACKET in 1 BOX / .9 g in 1 PACKET (0924-5701-01)

NDC Code 0924-5701-09

Package Description: 10 PACKET in 1 BOX / .9 g in 1 PACKET (0924-5701-01)

NDC Code 0924-5701-10

Package Description: 12 PACKET in 1 BOX / .9 g in 1 PACKET (0924-5701-01)

NDC Code 0924-5701-11

Package Description: 25 PACKET in 1 BOX / .9 g in 1 PACKET (0924-5701-01)

NDC Code 0924-5701-12

Package Description: 144 PACKET in 1 BOX / .9 g in 1 PACKET (0924-5701-01)

NDC Code 0924-5701-13

Package Description: 60 PACKET in 1 BOX / .9 g in 1 PACKET (0924-5701-01)

Product Details

What is NDC 0924-5701?

The NDC code 0924-5701 is assigned by the FDA to the product First Aid And Burn which is product labeled by Acme United Corporation. The product's dosage form is . The product is distributed in 12 packages with assigned NDC codes 0924-5701-02 6 packet in 1 bag / .9 g in 1 packet (0924-5701-01), 0924-5701-03 6 packet in 1 bag / .9 g in 1 packet (0924-5701-01), 0924-5701-04 10 packet in 1 box / .9 g in 1 packet (0924-5701-01), 0924-5701-05 12 packet in 1 box / .9 g in 1 packet (0924-5701-01), 0924-5701-06 25 packet in 1 box / .9 g in 1 packet (0924-5701-01), 0924-5701-07 60 packet in 1 box / .9 g in 1 packet (0924-5701-01), 0924-5701-08 144 packet in 1 box / .9 g in 1 packet (0924-5701-01), 0924-5701-09 10 packet in 1 box / .9 g in 1 packet (0924-5701-01), 0924-5701-10 12 packet in 1 box / .9 g in 1 packet (0924-5701-01), 0924-5701-11 25 packet in 1 box / .9 g in 1 packet (0924-5701-01), 0924-5701-12 144 packet in 1 box / .9 g in 1 packet (0924-5701-01), 0924-5701-13 60 packet in 1 box / .9 g in 1 packet (0924-5701-01). 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 And Burn?

Adults and children 2 years of age and older: clean the affected area apply a small amount of this product to the area 1 to 3 times daily may be covered with a sterile bandage children under 2 years of age: consult a doctor

Which are First Aid And Burn UNII Codes?

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

Which are First Aid And Burn 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 And Burn?

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

* 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".