NDC 0498-4140 4140 First Aid Kit

4140 First Aid Kit - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
0498-4140
Proprietary Name:
4140 First Aid Kit
Non-Proprietary Name: [1]
4140 First Aid
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Honeywell Safety Products Usa, Inc.
Labeler Code:
0498
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date: [9]
09-13-2018
Listing Expiration Date: [11]
12-31-2025
Exclude Flag: [12]
N
Code Structure:
Code Navigator:

Product Packages

NDC Code 0498-4140-01

Package Description: 1 KIT in 1 KIT * 30 mL in 1 BOTTLE (0498-0100-01) * 1.4 mL in 1 PACKET (0498-0501-00) * .4 mL in 1 POUCH (0498-0733-00) * .3 mL in 1 POUCH (0498-0121-00) * 3.5 g in 1 PACKET (0498-0203-00)

Product Details

What is NDC 0498-4140?

The NDC code 0498-4140 is assigned by the FDA to the product 4140 First Aid Kit which is a human over the counter drug product labeled by Honeywell Safety Products Usa, Inc.. The generic name of 4140 First Aid Kit is 4140 first aid. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 0498-4140-01 1 kit in 1 kit * 30 ml in 1 bottle (0498-0100-01) * 1.4 ml in 1 packet (0498-0501-00) * .4 ml in 1 pouch (0498-0733-00) * .3 ml in 1 pouch (0498-0121-00) * 3.5 g in 1 packet (0498-0203-00). 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 4140 First Aid Kit?

Adults and children 2 years of age and older; apply to affected area not more than 3 to 4 times dailychildren under 2 years of age: ask a doctoryou may report a serious reaction to this product to 800-430-5490

Which are 4140 First Aid Kit UNII Codes?

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

Which are 4140 First Aid Kit 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 4140 First Aid Kit?

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:

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Product Footnotes

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[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 ("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".