NDC 73190-002 Waltz Free Hand Sanitizer Foam

Benzalkonium Chloride

NDC Product Code 73190-002

NDC 73190-002-02

Package Description: 50 mL in 1 BOTTLE, PUMP

NDC 73190-002-27

Package Description: 798 mL in 1 BAG

NDC Product Information

Waltz Free Hand Sanitizer Foam with NDC 73190-002 is a a human over the counter drug product labeled by Avkare, Inc. The generic name of Waltz Free Hand Sanitizer Foam is benzalkonium chloride. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Avkare, Inc

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.

Waltz Free Hand Sanitizer Foam 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.
  • 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: Avkare, Inc
Labeler Code: 73190
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: 08-16-2019 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: 12-31-2020 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 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Waltz Free Hand Sanitizer Foam Product Label Images

Waltz Free Hand Sanitizer Foam 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.


For external use only.

Do Not Use In The Eyes.

In case of eye contact, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor

If irritation or redness develops or if condition persists more than 72 hours.

Keep Out Of Reach Of Children.

Instruct children on proper use. If swallowed, get medical help or contact a Poison Control Center right away.


Apply a small amount on your hands. Rub hands together until dry. When hands are visibly soiled, wash with soap and water. Store in cool, dry area.

Inactive Ingredients

Aloe Barbadensis Leaf Extract, Avena Sativa (Oat) Extract, Behentrimonium Methosulfate, Butylene Glycol, Caprylyl Glycol, Centrimonium Chloride, Dimethicone, Emulsifying Wax NF, Glycerin, Hydrolyzed Soy Protein, Mentha Piperita (Peppermint) Essential Oil, Phenoxyethanol, Retinyl Palmitate Vitamin A, Simmondsia Chinensis (Jojoba) Seed Oil, Sorbic Acid, Tetrasodium EDTA, Tocopheryl Acetate Vitamin E, Water

* Please review the disclaimer below.