NDC 81925-001 Hand Sanit1zing Wipes


NDC Product Code 81925-001

NDC 81925-001-01

Package Description: 50 PACKET in 1 PACKAGE > .1 CLOTH in 1 PACKET

NDC Product Information

Hand Sanit1zing Wipes with NDC 81925-001 is a a human over the counter drug product labeled by Zhejiang Healyou Hygienics Technology Co., Ltd.. The generic name of Hand Sanit1zing Wipes is wipes. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Zhejiang Healyou Hygienics Technology Co., Ltd.

Dosage Form: Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.

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 Sanit1zing Wipes 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: Zhejiang Healyou Hygienics Technology Co., Ltd.
Labeler Code: 81925
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: 05-18-2021 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.

Hand Sanit1zing Wipes Product Label Images

Hand Sanit1zing Wipes 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

Benzalkonium Chloride

Otc - Purpose



Use for hand sanitizing to reduce bacteria on the skin.


For external use only.When using this product

Otc - Stop Use

Lf irritation appears, stop use.

Otc - Do Not Use

Keep out of eyes.In case of contact, rinse eyes with water.

Otc - Ask Doctor

Consult a doctor if irritation persists more than 72 hours.

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

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children, except with adult supervision.


Thoroughly wipe hands and face as desired.

Allow to dry without wiping.

Discard wipe in trash receptacle after use.Do not flush.

Inactive Ingredient

Water(Aqua),Polyhexamethylene biguanide hydrochloride,Benzalkonium Chloride,Didecyldimethylammoniumchloride,Cetylpyridinium Chloride,monohydrate,Ethylhexylglycerin,Aloe Barbadensis Leaf Extract,Glycerine.

Storage And Handling

Store at room temperature

* Please review the disclaimer below.