NDC 74743-013 Rinse Free Antibacterial Hand Sanitizer Gel

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:
74743-013
Proprietary Name:
Rinse Free Antibacterial Hand Sanitizer Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
74743
Start Marketing Date: [9]
04-09-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 74743-013?

The NDC code 74743-013 is assigned by the FDA to the product Rinse Free Antibacterial Hand Sanitizer Gel which is product labeled by Guangzhou Joy Claire Biological Technology Co., Ltd. The product's dosage form is . The product is distributed in 19 packages with assigned NDC codes 74743-013-01 30 ml in 1 bottle , 74743-013-02 50 ml in 1 bottle , 74743-013-03 60 ml in 1 bottle , 74743-013-04 100 ml in 1 bottle , 74743-013-05 250 ml in 1 bottle , 74743-013-06 300 ml in 1 bottle , 74743-013-07 400 ml in 1 bottle , 74743-013-08 500 ml in 1 bottle , 74743-013-09 118 ml in 1 bottle , 74743-013-10 118 ml in 1 bottle , 74743-013-11 120 ml in 1 bottle , 74743-013-12 120 ml in 1 bottle , 74743-013-13 236 ml in 1 bottle , 74743-013-14 750 ml in 1 bottle , 74743-013-15 1000 ml in 1 bottle , 74743-013-16 2500 ml in 1 bottle , 74743-013-17 3800 ml in 1 bottle , 74743-013-18 4500 ml in 1 bottle , 74743-013-19 5000 ml in 1 bottle . 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 Rinse Free Antibacterial Hand Sanitizer Gel?

Open the cap and gently squeeze product into palm of hands,then rub thoroughly over all surfaces of both hands.

What is the NDC to RxNorm Crosswalk for Rinse Free Antibacterial Hand Sanitizer Gel?

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".