NDC 79606-002 Alcohol-based Disinfectant Hand Sanitizer

Alcohol-based Disinfectant Hand Sanitizer

NDC Product Code 79606-002

NDC 79606-002-01

Package Description: 60 mL in 1 BOTTLE

NDC 79606-002-02

Package Description: 120 mL in 1 BOTTLE

NDC 79606-002-03

Package Description: 236 mL in 1 BOTTLE

NDC 79606-002-04

Package Description: 250 mL in 1 BOTTLE

NDC 79606-002-05

Package Description: 300 mL in 1 BOTTLE

NDC 79606-002-06

Package Description: 500 mL in 1 BOTTLE

NDC 79606-002-07

Package Description: 1000 mL in 1 BOTTLE

NDC 79606-002-08

Package Description: 2000 mL in 1 BOTTLE

NDC 79606-002-09

Package Description: 3000 mL in 1 BOTTLE

NDC 79606-002-10

Package Description: 4000 mL in 1 BOTTLE

NDC 79606-002-11

Package Description: 5000 mL in 1 BOTTLE

NDC Product Information

Alcohol-based Disinfectant Hand Sanitizer with NDC 79606-002 is a a human over the counter drug product labeled by Foshan Lang-yeon Trade Limited Company. The generic name of Alcohol-based Disinfectant Hand Sanitizer is alcohol-based disinfectant hand sanitizer. The product's dosage form is gel and is administered via topical form.

Labeler Name: Foshan Lang-yeon Trade Limited Company

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.

Alcohol-based Disinfectant 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 80 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)

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: Foshan Lang-yeon Trade Limited Company
Labeler Code: 79606
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: 07-10-2020 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.

Alcohol-based Disinfectant 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(S)

Ethyl Alcohol 75% v/v. Purpose: Antimicrobial


Purpose: Antimicrobial , Hand Sanitizer


Pour a suitable amount of gel onto the palm of your hand and rub hands together thoroughly. Gel will evaporate. No need to rinse or dry hands after use


Keep out of reach of children This product is highly flammable Keep away from open flame or fire Avoid contact with eyes and mucous membranes Harmful if swallowed

Do Not Use


Otc - When Using


Otc - Stop Use



This product has a strong inhibitoryffect on various bacteria and virusesincluding Staphylococcus Aureus,Pseudomonas Aeruginosa, CandidaAlbcans and Escherichia Coli

Other Information

Keep in a cool, dry and well ventilated area away from direct sunlight

Inactive Ingredients

Water, Glycerin, Carbomer,Triethanolamine, Lavender Essence

* Please review the disclaimer below.