NDC 54860-351 Antibacterial Hand Sanitizer Original 1000ml 01

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:
54860-351
Proprietary Name:
Antibacterial Hand Sanitizer Original 1000ml 01
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Shenzhen Lantern Scicence Co Ltd
Labeler Code:
54860
Start Marketing Date: [9]
04-18-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 54860-351-01

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 54860-351?

The NDC code 54860-351 is assigned by the FDA to the product Antibacterial Hand Sanitizer Original 1000ml 01 which is product labeled by Shenzhen Lantern Scicence Co Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54860-351-01 1000 ml in 1 bottle, plastic . 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 Antibacterial Hand Sanitizer Original 1000ml 01?

Place enough product in your palm. rub hands vigorously until dry.children under 6 years of age should be supervised when using this product.

What is the NDC to RxNorm Crosswalk for Antibacterial Hand Sanitizer Original 1000ml 01?

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".