NDC 73126-032 Truth Antibacterial Foaming Hand Wash - Unscented

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)

• BENZALKONIUM CHLORIDE .13 g/100mL

Inactive Ingredient(s)

• WATER (UNII: 059QF0KO0R)
• SODIUM CHLORIDE (UNII: 451W47IQ8X)
• COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
• LAURAMINE OXIDE (UNII: 4F6FC4MI8W)
• DISODIUM COCOAMPHODIPROPIONATE (UNII: 6K8PRP397M)
• GLYCERIN (UNII: PDC6A3C0OX)
• METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)

Administration Route(s)

• 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

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.