NDC 80974-001 Instant Sanitizing Soft Wipes


NDC Product Code 80974-001

NDC 80974-001-01

Package Description: 1 APPLICATOR in 1 BAG > 5 g in 1 APPLICATOR

NDC 80974-001-02

Package Description: 20 APPLICATOR in 1 BAG > 5 g in 1 APPLICATOR

NDC 80974-001-03

Package Description: 50 APPLICATOR in 1 BAG > 5 g in 1 APPLICATOR

NDC 80974-001-04

Package Description: 80 APPLICATOR in 1 BAG > 5 g in 1 APPLICATOR

NDC 80974-001-05

Package Description: 60 APPLICATOR in 1 CANISTER > 5 g in 1 APPLICATOR

NDC 80974-001-06

Package Description: 100 APPLICATOR in 1 CANISTER > 5 g in 1 APPLICATOR

NDC 80974-001-07

Package Description: 160 APPLICATOR in 1 CANISTER > 5 g in 1 APPLICATOR

NDC Product Information

Instant Sanitizing Soft Wipes with NDC 80974-001 is a a human over the counter drug product labeled by Guangdong Kingfa Sci.&tech.co.,ltd.. The generic name of Instant Sanitizing Soft Wipes is alcohol. The product's dosage form is swab and is administered via topical form.

Labeler Name: Guangdong Kingfa Sci.&tech.co.,ltd.

Dosage Form: Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab 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.

Instant Sanitizing Soft 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.

  • ALCOHOL 75 g/100g

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: Guangdong Kingfa Sci.&tech.co.,ltd.
Labeler Code: 80974
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: 12-15-2020 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.

Instant Sanitizing Soft 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

Active Ingredient(S)

Alcohol 75% v/v.


Purpose: Antimicrobial


For sanitizing to help reduce bacteria on the skin.


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

Otc - When Using

When using this product, avoid contact with eyes.

Do Not Use

In or near the eyes. In case of contact, rinse eyes thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or rash appears and lasts.

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.


  • Rub thoroughly over all surfaces of both hands with wipe. Allow to dry without wiping.Keep away from dirct sunlight; store in a cool, dry place.

Other Information

  • Store below 104F(40C)May discolor certain fabrics.Don't put it in the car, keep away from high temperature.

Inactive Ingredients


* Please review the disclaimer below.