NDC 76992-004 Hand Rub

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:
76992-004
Proprietary Name:
Hand Rub
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Alchemical Solutions, Llc
Labeler Code:
76992
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 76992-004-01

Package Description: 1 SPRAY in 1 JUG

NDC Code 76992-004-02

Package Description: 5 SPRAY in 1 PAIL

NDC Code 76992-004-03

Package Description: 55 SPRAY in 1 DRUM

NDC Code 76992-004-04

Package Description: 270 SPRAY in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK

NDC Code 76992-004-05

Package Description: 350 SPRAY in 1 TANK

Product Details

What is NDC 76992-004?

The NDC code 76992-004 is assigned by the FDA to the product Hand Rub which is product labeled by Alchemical Solutions, Llc. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 76992-004-01 1 spray in 1 jug , 76992-004-02 5 spray in 1 pail , 76992-004-03 55 spray in 1 drum , 76992-004-04 270 spray in 1 container, flexible intermediate bulk , 76992-004-05 350 spray in 1 tank . 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 Rub?

Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Hand Rub UNII Codes?

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

Which are Hand Rub 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".