NDC 44224-1000 Adventure Medical Kits 1 Person First Aid

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:
44224-1000
Proprietary Name:
Adventure Medical Kits 1 Person First Aid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
44224
Start Marketing Date: [9]
08-25-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 44224-1000?

The NDC code 44224-1000 is assigned by the FDA to the product Adventure Medical Kits 1 Person First Aid which is product labeled by Tender Corp Dba Adventure Medical Kits. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44224-1000-1 1 kit in 1 kit * .5 ml in 1 package (52124-0008-1) * .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 Adventure Medical Kits 1 Person First Aid?

For professional and hospital use. helps prevent infection. antiseptic cleansing of face hand and body without soap and water. Use: For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

Which are Adventure Medical Kits 1 Person First Aid UNII Codes?

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

Which are Adventure Medical Kits 1 Person 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 Adventure Medical Kits 1 Person 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:

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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".