NDC 73788-004 Hand Sanitizer

Ethyl Alcohol

NDC Product Code 73788-004

NDC 73788-004-01

Package Description: 200 BOTTLE in 1 CARTON > 30 mL in 1 BOTTLE

NDC 73788-004-02

Package Description: 150 BOTTLE in 1 CARTON > 60 mL in 1 BOTTLE

NDC 73788-004-03

Package Description: 100 BOTTLE in 1 CARTON > 100 mL in 1 BOTTLE

NDC 73788-004-04

Package Description: 24 BOTTLE in 1 CARTON > 237 mL in 1 BOTTLE

NDC 73788-004-05

Package Description: 20 BOTTLE in 1 CARTON > 500 mL in 1 BOTTLE

NDC 73788-004-06

Package Description: 18 BOTTLE in 1 CARTON > 1000 mL in 1 BOTTLE

NDC Product Information

Hand Sanitizer with NDC 73788-004 is a a human over the counter drug product labeled by Hangzhou Huiji Biotechnology Co., Ltd.. The generic name of Hand Sanitizer is ethyl alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Hangzhou Huiji Biotechnology Co., Ltd.

Dosage Form: Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.

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.

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.

  • ALCOHOL 75 mL/100mL

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)
  • CARBOMER 934 (UNII: Z135WT9208)

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: Hangzhou Huiji Biotechnology Co., Ltd.
Labeler Code: 73788
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: 05-29-2020 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: 12-31-2021 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.

Hand Sanitizer Product Label Images

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

Active Ingredient

Ethyl Alcohol 75%




■ Hand sanitizer to help decrease bacteria on

the skin

■When water, soap & towel are not


■Recommended for repeated use,


For external use only■Highly inflammable

Keep away from heat, sparks, open flame, hot surfaces.

Do not apply around eyes. Do not use in ears & mouth.

Avoid contact with eyes

If in eyes: rinse well with clean water

Stop use and seek medical advice or attention if

irritation persists

Keep Out Of Reach Of Children

Keep out of reach of children. Children must be

supervised in use of this product


■Squeeze the bottle after removing the lid and thoroughly

spread on both hands. Rub into skin until dry

Other Information Avoid contact with fabrics as

could cause discolouration

Inactive Ingredients

Water, Glycerin, Aloe

barbadensis leaf extract, Carbomer.

Tocopheryl Acetate, Triethanolamine

* Please review the disclaimer below.