NDC 79091-011 Hand Sanitizer Refill

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:
79091-011
Proprietary Name:
Hand Sanitizer Refill
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Haan Brand Sl
Labeler Code:
79091
Start Marketing Date: [9]
09-23-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 79091-011-01

Package Description: 100 mL in 1 POUCH

Product Details

What is NDC 79091-011?

The NDC code 79091-011 is assigned by the FDA to the product Hand Sanitizer Refill which is product labeled by Haan Brand Sl. The product's dosage form is . The product is distributed in a single package with assigned NDC code 79091-011-01 100 ml in 1 pouch . 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 Hand Sanitizer Refill?

Directions: Wet hands throughly with product and allow to dry without wiping For Children under 6 years of age do not use without supervision of an adult. Not recomended for infants

Which are Hand Sanitizer Refill UNII Codes?

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

Which are Hand Sanitizer Refill 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:

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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".