NDC 67676-006 Bzk Alcohol Free Hand Sanitizer

Benzalkonium Chloride Liquid Topical

NDC Product Information

Bzk Alcohol Free Hand Sanitizer with NDC 67676-006 is a human over the counter drug product labeled by Sarati International, Inc.. The generic name of Bzk Alcohol Free Hand Sanitizer is benzalkonium chloride. The product's dosage form is liquid and is administered via topical form.

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.

Bzk Alcohol Free Hand Sanitizer 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.

RxNorm Crosswalk

What is RxNorm?
RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) (RxCUI) to each NDC.

The RxNorm Crosswalk for this NDC code indicates a single concept unique identifier (RXCUI) is associated with this product:

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)
  • LAURETH-4 (UNII: 6HQ855798J)

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: Sarati International, Inc.
Labeler Code: 67676
FDA Application Number: part333A 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: 03-31-2021 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2022 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.

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.

Bzk Alcohol Free Hand Sanitizer Product Label Images

Bzk Alcohol Free Hand Sanitizer 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


Drug Facts

Otc - Active Ingredient

Active Ingredient:Benzalkonium Chloride 0.13%

Otc - Purpose

Purpose:Hand & Skin Sanitizer

Indications & Usage

Uses: BZK™ Alcohol Free Hand Sanitizer provides revolutionaryprotection in an alcohol-free formula. The scientifically-provensolution kills harmful germs, bacteria, and microbes, and gentlysoothes and softens skin with aloe vera. Recommended forrepeated use.


Warnings: Do not freeze + For external use only + Do not use inears, eyes or mouth + When using this product, avoid contactwith the eyes + In case of contact, flush eyes with water + Stopuse and ask a doctor if redness or irritation develops and persistsfor more than 72 hours

Otc - Keep Out Of Reach Of Children

+ Keep out of reach of children + Childrenshould be supervised when using this product.

Dosage & Administration

Directions: Apply liberally to the palms of the hands or areas ofdamaged skin. Rub into skin until dry. Recommended forrepeated use.

Other Safety Information

Other Information: Store in a cool dry place below 104°F(40°C).

Inactive Ingredient

Inactive Ingredients: Aloe Barbadensis leaf extract, Aqua,Citric Acid, Caprylyl Glucoside, Laureth-4, Polyhexanide,Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

Otc - Questions

Questions? 1-800-920-7650 Mon-Fri 10AM-4PM (EST)

Product Label

BZK™Alcohol FreeHand SanitizerUP TO 4 HOURS OF PROTECTION + Killsup to 99.9% of Harmful Germs andBacteria + Naturally Derived, Alcohol andBleach Free + Gentle and Non-stingingwith Aloe Vera1.7 FL OZ (50 ML)MADE IN THE USABZK™ products are manufactured understrict quality guidelines under 21 CFR ata cGMP FDA-registered site.Distributed By BZK HealthBuffalo NY, 14221bzkhealth.com​1.7 FL OZ2 FL OZrres

* Please review the disclaimer below.