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  4. NDC Product Code: 0924-1806 Acme First Aid Contains 404 Pieces

NDC 0924-1806 Acme First Aid Contains 404 Pieces

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0924-1806?
  5. Acme First Aid Contains 404 Pieces 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.

Get all the details for National Drug Code (NDC) 0924-1806 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:
0924-1806
Proprietary Name:
Acme First Aid Contains 404 Pieces
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Acme United Corp.
Labeler Code:
0924
Product Label ID:
106eb41d-f74b-4975-945f-671f15e9343a
FDA Application Number: [6]
part333
Marketing Category: [8]
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date: [9]
04-27-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331 - ORANGE)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
ASPIRIN
Score:
1

Code Structure Chart

Product Details

What is NDC 0924-1806?

The NDC code 0924-1806 is assigned by the FDA to the product Acme First Aid Contains 404 Pieces which is product labeled by Acme United Corp.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0924-1806-01 1 kit in 1 kit * .5 g in 1 tube (52124-0003-1) * 2 tablet, chewable in 1 package (52124-0012-1) * .5 ml in 1 package (52124-0008-1) * .5 ml in 1 package (52124-0002-1) * 10 ml in 1 bottle (52124-0005-1) * .8 ml in 1 package (52124-0001-1) * .9 g in 1 package (52124-0004-1). 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 Acme First Aid Contains 404 Pieces?

This product is used as Purpose: First aid antiseptic, external analgesicUses: First aid to help prevent infection and for the temporary relief of pain and itching associated with: Minor CutsScrapesBurns Use: For Professional and Hospital use.  Helps prevent infection.  Antiseptic cleansing of face, hands and body without soap and water. Uses:  To help prevent infection in: minor cuts;  scrapes;  burns Uses:For flushing or irrigating the eyes toremove loose foreign material, air pollutants, or chlorinated water. Use:    For preparation of skin before injection. Use: For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites. Usestemporary relief of minor aches, pains and headachesto reduce fever associated with colds, sore throats, teething

Which are Acme First Aid Contains 404 Pieces UNII Codes?

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

Which are Acme First Aid Contains 404 Pieces 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 Acme First Aid Contains 404 Pieces?

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: 1038561 - benzalkonium Cl 0.4 % Medicated Pad
  • RxCUI: 1038561 - benzalkonium chloride 4 MG/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".