NDC 73126-032 Truth Antibacterial Foaming Hand Wash - Unscented

Benzalkonium Chloride

NDC Product Code 73126-032

NDC 73126-032-01

Package Description: 60 mL in 1 BOTTLE

NDC 73126-032-02

Package Description: 88 mL in 1 BOTTLE

NDC 73126-032-03

Package Description: 237 mL in 1 BOTTLE

NDC 73126-032-04

Package Description: 355 mL in 1 BOTTLE

NDC 73126-032-05

Package Description: 474 mL in 1 BOTTLE

NDC 73126-032-06

Package Description: 591 mL in 1 PACKAGE

NDC 73126-032-07

Package Description: 710 mL in 1 PACKAGE

NDC 73126-032-08

Package Description: 947 mL in 1 PACKAGE

NDC Product Information

Truth Antibacterial Foaming Hand Wash - Unscented with NDC 73126-032 is a 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 RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1046593.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug 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.

Truth Antibacterial Foaming Hand Wash - Unscented Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)

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.

Labeler Name: Lab-clean, Inc
Labeler Code: 73126
FDA Application Number: part333E 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.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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.

Start Marketing Date: 03-04-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 04-20-2024 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.

Exclude Flag: N - NO 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".

* Please review the disclaimer below.

Truth Antibacterial Foaming Hand Wash - Unscented Product Label Images

Truth Antibacterial Foaming Hand Wash - Unscented Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredient

Benzalkonium Chloride  0.13%




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


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.


  • 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.

* Please review the disclaimer below.