NDC 74247-0012 Hanna Hand Sanitizer

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:
74247-0012
Proprietary Name:
Hanna Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rainbow Co Ltd
Labeler Code:
74247
Start Marketing Date: [9]
06-13-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 74247-0012-1

Package Description: 500 mL in 1 BOTTLE

NDC Code 74247-0012-2

Package Description: 300 mL in 1 BOTTLE

NDC Code 74247-0012-3

Package Description: 55 mL in 1 BOTTLE

NDC Code 74247-0012-4

Package Description: 100 mL in 1 BOTTLE

NDC Code 74247-0012-5

Package Description: 2000 mL in 1 BOTTLE

NDC Code 74247-0012-6

Package Description: 5000 mL in 1 BOTTLE

NDC Code 74247-0012-7

Package Description: 3 mL in 1 POUCH

Product Details

What is NDC 74247-0012?

The NDC code 74247-0012 is assigned by the FDA to the product Hanna Hand Sanitizer which is product labeled by Rainbow Co Ltd. The product's dosage form is . The product is distributed in 7 packages with assigned NDC codes 74247-0012-1 500 ml in 1 bottle , 74247-0012-2 300 ml in 1 bottle , 74247-0012-3 55 ml in 1 bottle , 74247-0012-4 100 ml in 1 bottle , 74247-0012-5 2000 ml in 1 bottle , 74247-0012-6 5000 ml in 1 bottle , 74247-0012-7 3 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 Hanna Hand Sanitizer?

Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.Supervise children in the use of this product.

Which are Hanna Hand Sanitizer UNII Codes?

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

Which are Hanna Hand Sanitizer 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 Hanna Hand Sanitizer?

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".