NDC 73943-949 Han-san Gel With Aloe


NDC Product Code 73943-949

NDC 73943-949-01

Package Description: 59.14 mL in 1 BOTTLE

NDC 73943-949-02

Package Description: 118.29 mL in 1 BOTTLE

NDC 73943-949-03

Package Description: 354.88 mL in 1 BOTTLE

NDC 73943-949-04

Package Description: 591.47 mL in 1 BOTTLE

NDC 73943-949-05

Package Description: 2000 mL in 1 BOTTLE

NDC 73943-949-06

Package Description: 3785.41 mL in 1 BOTTLE

NDC 73943-949-07

Package Description: 208198 mL in 1 DRUM

NDC Product Information

Han-san Gel With Aloe with NDC 73943-949 is a a human over the counter drug product labeled by Rite-kem Incorporated. The generic name of Han-san Gel With Aloe is alcohol. The product's dosage form is gel and is administered via topical form.

Labeler Name: Rite-kem Incorporated

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.

Han-san Gel With Aloe 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 70 mL/100mL

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: Rite-kem Incorporated
Labeler Code: 73943
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: 03-15-2021 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.

Han-san Gel With Aloe Product Label Images

Han-san Gel With Aloe 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

Otc - Active Ingredient

Alcohol 70%

Otc - Purpose


Indications & Usage

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.


For external use only. Flammable. Keep away from heat or flame

Otc - Do Not Use

  • In children less than 2 months of ageon open skin wounds

Otc - Stop Use

Stop use and ask a doctor if irritiation or rash occurs. These may be signs of serious condition

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a poison control center right away.

Dosage & Administration

  • Directions.Place enough product on hands to cover all surfaces. Rub together until dry.Suerpvise children under 6 years of age when using this product to avoid swallowing.

Other Safety Information

Other informationstore between 15-30 c (59-86F)Avoid freezing and excessing heat above 40 c (104F)

Inactive Ingredient

Inactive ingredients: glycerin, hydrogen peroxide, purified water USP

* Please review the disclaimer below.