NDC 79903-165 Moisturizing Antibacterial
Benzalkonium Chloride Soap Topical

Product Information

What is NDC 79903-165?

The NDC code 79903-165 is assigned by the FDA to the product Moisturizing Antibacterial which is a human over the counter drug product labeled by Wal-mart Stores, Inc.,. The generic name of Moisturizing Antibacterial is benzalkonium chloride. The product's dosage form is soap and is administered via topical form. The product is distributed in a single package with assigned NDC code 79903-165-50 1470 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, RxNorm crosswalk and the complete product label.

NDC Product Code79903-165
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Moisturizing Antibacterial
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Benzalkonium Chloride
Product Type What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Human Otc Drug
Dosage FormSoap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.
Administration Route(s) What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Wal-mart Stores, Inc.,
Labeler Code79903
FDA Application Number What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
part333A
Marketing Category What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
12-15-2022
Listing Expiration Date 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.
12-31-2024
Exclude Flag 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".
N
NDC Code Structure

What are the uses for Moisturizing Antibacterial?


Product Packages

NDC Code 79903-165-50

Package Description: 1470 mL in 1 BOTTLE, PLASTIC

Product Details

What are Moisturizing Antibacterial Active Ingredients?

An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

Moisturizing Antibacterial Active Ingredients UNII Codes

NDC to RxNorm Crosswalk

What is RxNorm? 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:
  • RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap

Moisturizing Antibacterial Inactive Ingredients UNII Codes

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

* Please review the disclaimer below.

Moisturizing Antibacterial Product Label

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Label Table of Contents



Inactive Ingredient



Benzalkonium chloride 0.13%


Purpose



Antibacterial


Use



For handwashing to decrease bacteria on the skin


Warnings



For external use only:hands only


When Using This Product



  • avoid contact with eyes.  If contact occurs, rinse eyes thoroughly with water

Stop Use And Ask A Doctor If



  • irritation or redness develops
  • condition persists for more than 72 hours

Keep Out Of Reach Of Children.



If swallowed, get medical help or contact a Poison Control Center right away.


Directions



  • wet hands
  • apply palmful to hands
  • scrub thoroughly
  • rinse thoroughly

Inactive Ingredients



water, lauramine oxide, cocamidopropyl betaine, lauramidopropylamine oxide, sodium chloride, myristamidopropylamine oxide, glycerin, fragrance, disteareth-75 IPDI, PEG-150 distearate, citric acid, tetrasodium EDTA, benzophenone-4, sodium benzoate, Citrus nobilis (mandarin orange) oil, Camellia sinensis leaf extract, Zingiber officinale (ginger) root oil, blue 1, yellow 5


Other



Satisfaction guaranteed. For questions or comments please call 1-888-287-1915

DISTRIBUTED BY: Wal-Mart Stores, Inc.,

Bentonville, AR 72716

This product is not manufactured or distributed by Colgate-Palmolive Company, distributor of Softsoap Antibacterial Hand Soap with Moisturizers Fresh Citrus*

Made in the USA with domestic and imported ingredients

Factory Certified


Principal Display Panel



equate

Compare to Softsoap Antibacterial Hand Soap with Moisturizers Fresh Citrus* active ingredient

Citrus

LIQUID HAND SOAP

ANTIBACTERIAL

With light moisturizers

Helps kill harmful germs

50 FL OZ (1 QT 1 PT 2 FL OZ) 1.47 L


* Please review the disclaimer below.