NDC 52473-010 Odorless Hand Sanitizer Foam

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:
52473-010
Proprietary Name:
Odorless Hand Sanitizer Foam
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tinks
Labeler Code:
52473
Start Marketing Date: [9]
05-15-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 52473-010-05

Package Description: 150 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 52473-010?

The NDC code 52473-010 is assigned by the FDA to the product Odorless Hand Sanitizer Foam which is product labeled by Tinks. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52473-010-05 150 ml in 1 bottle, pump . 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 Odorless Hand Sanitizer Foam?

UsesFor Hand sanitizing to decrease bacteria on the skinRecommended for repeated uses

Which are Odorless Hand Sanitizer Foam UNII Codes?

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

Which are Odorless Hand Sanitizer Foam 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 Odorless Hand Sanitizer Foam?

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".