NDC 78940-003 A1 American Defender Collection

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:
78940-003
Proprietary Name:
A1 American Defender Collection
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
78940
Start Marketing Date: [9]
07-15-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 78940-003?

The NDC code 78940-003 is assigned by the FDA to the product A1 American Defender Collection which is product labeled by Tiger Hospitality, Llc Dba A1 American. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 78940-003-01 1 bottle, plastic in 1 package / 2 ml in 1 bottle, plastic, 78940-003-02 5 bottle, plastic in 1 package / 2 ml in 1 bottle, plastic, 78940-003-03 10 bottle, plastic in 1 package / 2 ml in 1 bottle, plastic, 78940-003-04 25 bottle, plastic in 1 package / 2 ml in 1 bottle, plastic, 78940-003-05 80 bottle, plastic in 1 canister / 2 ml in 1 bottle, plastic. 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 A1 American Defender Collection?

Tear open packetOpen and unfold wipeThoroughly wipe hands, fingers and wristsDiscard aftersingle use

Which are A1 American Defender Collection UNII Codes?

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

Which are A1 American Defender Collection 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 A1 American Defender Collection?

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".