NDC 69558-001 Antimicrobial Alcohol Hand Wipes

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:
69558-001
Proprietary Name:
Antimicrobial Alcohol Hand Wipes
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Geri Gentile Corp
Labeler Code:
69558
Start Marketing Date: [9]
08-03-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69558-001-35

Package Description: 135 PATCH in 1 CANISTER / 3.37 g in 1 PATCH

Product Details

What is NDC 69558-001?

The NDC code 69558-001 is assigned by the FDA to the product Antimicrobial Alcohol Hand Wipes which is product labeled by Geri Gentile Corp. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69558-001-35 135 patch in 1 canister / 3.37 g in 1 patch. 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 Antimicrobial Alcohol Hand Wipes?

To start feed: Remove cover and discard seal from container, From center of toweled roll , pull up wipe corner; tear off fist wipe for use. Twist next wipe into a point and thread through the hole in the container cover.Pull through about one inch. Replace cover,Pull out wipes as needed and snap off at 90°angle. Keep cap closed to prevent moisture loss.Wipe hands, fingers, interdigital areas and wrists thoroughly with towelette. Be sure to utilize the entire wipe surface. Allow to dry.If hands are visibly soiled or contaminated, use first wipe to clean hands, then discard wipe, Sanitize with a second wipe.Discard after single use.

Which are Antimicrobial Alcohol Hand Wipes UNII Codes?

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

Which are Antimicrobial Alcohol Hand Wipes 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 Antimicrobial Alcohol Hand Wipes?

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".