NDC 73126-032 Truth Antibacterial Foaming Hand Wash - Unscented
Benzalkonium Chloride Liquid Topical

Product Information

What is NDC 73126-032?

The NDC code 73126-032 is assigned by the FDA to the UNFINISHED product Truth Antibacterial Foaming Hand Wash - Unscented which is a human over the counter drug product labeled by Lab-clean, Inc. The generic name of Truth Antibacterial Foaming Hand Wash - Unscented is benzalkonium chloride. The product's dosage form is liquid and is administered via topical form. The product is distributed in 8 packages with assigned NDC codes 73126-032-01 60 ml in 1 bottle , 73126-032-02 88 ml in 1 bottle , 73126-032-03 237 ml in 1 bottle , 73126-032-04 355 ml in 1 bottle , 73126-032-05 474 ml in 1 bottle , 73126-032-06 591 ml in 1 package , 73126-032-07 710 ml in 1 package , 73126-032-08 947 ml in 1 package . 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 Code73126-032
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.		Truth Antibacterial Foaming Hand Wash - Unscented
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
Substance Name What is the Substance Name?
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.		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 FormLiquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.		Lab-clean, Inc
Labeler Code73126
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.		part333E
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.		03-04-2021
End Marketing Date What is the End Marketing Date?
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.		04-20-2024
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
Unfinished Product What is an Unfinished Product?
Not Available		Yes
NDC Code Structure

What are the uses for Truth Antibacterial Foaming Hand Wash - Unscented?


Product Packages

NDC Code 73126-032-01

Package Description: 60 mL in 1 BOTTLE

NDC Code 73126-032-02

Package Description: 88 mL in 1 BOTTLE

NDC Code 73126-032-03

Package Description: 237 mL in 1 BOTTLE

NDC Code 73126-032-04

Package Description: 355 mL in 1 BOTTLE

NDC Code 73126-032-05

Package Description: 474 mL in 1 BOTTLE

NDC Code 73126-032-06

Package Description: 591 mL in 1 PACKAGE

NDC Code 73126-032-07

Package Description: 710 mL in 1 PACKAGE

NDC Code 73126-032-08

Package Description: 947 mL in 1 PACKAGE

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

Product Details

What are Truth Antibacterial Foaming Hand Wash - Unscented 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.

Truth Antibacterial Foaming Hand Wash - Unscented 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

Truth Antibacterial Foaming Hand Wash - Unscented 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.

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Truth Antibacterial Foaming Hand Wash - Unscented 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



Active Ingredient



Benzalkonium Chloride  0.13%


Purpose



Antimicrobial


Uses



For hand sanitizing to decrease bacteria on the skin. Recommended for repeated use.


Warnings



For external use only.

When using this product, avoid contact with eyes. In case of eye contact flush eyes with water.Do not ingest.

Stop use and ask a doctor if irritation or redness develops and conditions persist.


Keep Out Of Reach Of Children.



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


Directions



  • Apply small amount of product to wet hands. Work into lather and rub briskly for 15-30 seconds. Rinse thoroughly. Dry hands.

Inactive Ingredients



Water, Sodium Chloride, Cocamidopropyl Betaine, Lauramine Oxide, Disodium Cocoamphodipropionate, Glycerin, Methylchloroisothiazolinone.


Product Label



image description - Image 1

image description - Image 1


* Please review the disclaimer below.