NDC 54860-369 Hand Sanitizer 59ml 02

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:
54860-369
Proprietary Name:
Hand Sanitizer 59ml 02
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]
05-11-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 54860-369-01

Package Description: 59 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 54860-369?

The NDC code 54860-369 is assigned by the FDA to the product Hand Sanitizer 59ml 02 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 54860-369-01 59 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 Hand Sanitizer 59ml 02?

Wet hands thoroughyly with product and rub until dry without wiping.For children under 6,use only under adult supervision.Not recommended for infants.

What is the NDC to RxNorm Crosswalk for Hand Sanitizer 59ml 02?

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".