NDC 0498-4289 4289 First Aid Kit
4289 First Aid Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0498 - Honeywell Safety Products Usa, Inc.
- 0498-4289 - 4289 First Aid Kit
Product Packages
NDC Code 0498-4289-01
Package Description: 1 KIT in 1 KIT * .9 g in 1 PACKET (0498-0750-35) * .4 mL in 1 POUCH (0498-0143-04) * 1.4 mL in 1 PACKET (0498-0501-00) * .4 mL in 1 POUCH (0498-0733-00) * 30 mL in 1 BOTTLE (0498-0100-01) * .6 mL in 1 VIAL * 3.5 g in 1 PACKET (0498-0203-00)
Product Details
What is NDC 0498-4289?
What are the uses for 4289 First Aid Kit?
What is the NDC to RxNorm Crosswalk for 4289 First Aid Kit?
- RxCUI: 1011852 - lidocaine HCl 2 % Topical Gel
- RxCUI: 1011852 - lidocaine hydrochloride 0.02 MG/MG Topical Gel
- RxCUI: 1011852 - lidocaine hydrochloride 2 % Topical Jelly
- RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
- RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
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[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".