NDC 75139-006 Ancos Silver Ion Hand Sanitizer

Ancos Silver Ion Hand Sanitizer

NDC Product Code 75139-006

NDC 75139-006-01

Package Description: 100 mL in 1 BOTTLE

NDC 75139-006-02

Package Description: 500 mL in 1 BOTTLE

NDC Product Information

Ancos Silver Ion Hand Sanitizer with NDC 75139-006 is a a human over the counter drug product labeled by Anson Bio-technology Co., Ltd.. The generic name of Ancos Silver Ion Hand Sanitizer is ancos silver ion hand sanitizer. The product's dosage form is gel and is administered via topical form.

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.

Ancos Silver Ion 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.

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.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Anson Bio-technology Co., Ltd.
Labeler Code: 75139
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: 04-28-2020 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 - 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.

Ancos Silver Ion Hand Sanitizer Product Label Images

Ancos Silver Ion 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

Main Active Ingredients And Content

Silver ion: 0.01%, Ethyl alcohol: 62%(v/v)




The product has antibacterial effect on E coli, Staphylococcus aureus and Candida albicans, and can be used for hand disinfection in places such as intensive care unit, outpatient service, emergency room, ward and clinics, as well as in environment such as home and social places, especially when water is not available


Hand hygiene and disinfection: Take an appropriate amount of disinfectant to the palm, rub according to the hand disinfection code instructions, ensure that the sanitizer completely covers the skin of the hand sand wait for one minute until dry


  • Sanitizer for external use, shall not betaken orally and shall be placed out of children's reach.Avoid using with antagonist drugsThose with allergies shall use

Other Tips

Protect from light and store airtight at room temperature


Do not use this product in or near the eyes In case of contact, rinse eyes If irritation or rash appears and persists, stop using and consult the doctor.Please place out of children's reach. If swallowed, seek medical help or contact a Poison Control Center immediately

Other Ingredients

Purified water, Glycerol, Carbomer, Menthol

* Please review the disclaimer below.