NDC 34839-003 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:
34839-003
Proprietary Name:
Hand Sanitizer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Round Bridge Inc
Labeler Code:
34839
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 34839-003-01

Package Description: 59 mL in 1 BOTTLE

NDC Code 34839-003-02

Package Description: 118 mL in 1 BOTTLE

NDC Code 34839-003-03

Package Description: 236 mL in 1 BOTTLE

NDC Code 34839-003-04

Package Description: 500 mL in 1 BOTTLE

Product Details

What is NDC 34839-003?

The NDC code 34839-003 is assigned by the FDA to the product Hand Sanitizer which is product labeled by Round Bridge Inc. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 34839-003-01 59 ml in 1 bottle , 34839-003-02 118 ml in 1 bottle , 34839-003-03 236 ml in 1 bottle , 34839-003-04 500 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 Hand Sanitizer?

Place enough product on hands to cover all surfaces. Rub hands together until dry.Children under 6 years of age should be supervised when using this product.

What is the NDC to RxNorm Crosswalk for 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".