NDC 49035-177 Equate Antibacterial Foaming

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:
49035-177
Proprietary Name:
Equate Antibacterial Foaming
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wal-mart Stores Inc
Labeler Code:
49035
Start Marketing Date: [9]
08-24-2010
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)

Product Packages

NDC Code 49035-177-08

Package Description: 222 mL in 1 BOTTLE, PUMP

Product Details

What is NDC 49035-177?

The NDC code 49035-177 is assigned by the FDA to the product Equate Antibacterial Foaming which is product labeled by Wal-mart Stores Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 49035-177-08 222 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 Equate Antibacterial Foaming?

Apply onto dry hands, work into a lather vigorously. Rinse thoroughly.

Which are Equate Antibacterial Foaming UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Equate Antibacterial Foaming?

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".