NDC 74032-750 Azusa Safety Hand Sanitizer

Product Information

Product Packages

NDC 74032-750-01

Package Description: 50 mL in 1 BOTTLE, PLASTIC

NDC 74032-750-02

Package Description: 60 mL in 1 BOTTLE, PLASTIC

NDC 74032-750-03

Package Description: 100 mL in 1 BOTTLE, PLASTIC

NDC 74032-750-04

Package Description: 225 mL in 1 BOTTLE, PLASTIC

NDC 74032-750-05

Package Description: 350 mL in 1 BOTTLE, PLASTIC

NDC 74032-750-06

Package Description: 500 mL in 1 BOTTLE, PLASTIC

NDC 74032-750-07

Package Description: 1000 mL in 1 BOTTLE, PLASTIC

NDC 74032-750-08

Package Description: 5000 mL in 1 BOTTLE, PLASTIC

NDC 74032-750-09

Package Description: 1200 mL in 1 BOTTLE, PLASTIC

NDC 74032-750-10

Package Description: 4800 mL in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Azusa Safety Hand Sanitizer is product labeled by Azusa Safety, Inc.. The product's dosage form is and is administered via form.

What are Azusa Safety Hand Sanitizer Active Ingredients?

The following is the list of active ingredients in this product. 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.

  • ALCOHOL (UNII: 3K9958V90M)
  • ALCOHOL (UNII: 3K9958V90M) (Active Moiety)

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 code indicates a single concept unique identifier (RXCUI) is associated with this product:

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)

* Please review the disclaimer below.

Azusa Safety Hand Sanitizer Labeling and Warnings

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.

Table of Contents

Drug Facts

Active Ingredient

Ethyl Alcochol 75%




to decrease bacteria on the skin that could cause skin disease.


For external use only-hands

Flammable, keep away from heat or flame.

When using this product

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • do not inhale or ingest
  • Stop use and ask doctor if irritation or redness develop

Keep Out Of Reach Of Children.

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


  • wet hands thoroughly with product and allow to dry without wiping
  • for children under 6, use only under adult supervision

Inactive Ingredients

water, carbomer, glycerin, fragrance


KILLS 99.99% *

Dist. by Azusa Safety, Inc. 1299 W. State
St Ontario, CA 91762

*Effective at eliminating more than 99.99% of many common harmful germs and bacteria in as little as 15 seconds.

Made in China

* Please review the disclaimer below.