NDC 78122-102 Alcohol Wet Wipes

Alcohol Wipes

NDC Product Code 78122-102

NDC 78122-102-13

Package Description: 40 CLOTH in 1 BAG

NDC 78122-102-15

Package Description: 50 CLOTH in 1 BAG

NDC 78122-102-21

Package Description: 80 CLOTH in 1 BAG

NDC 78122-102-25

Package Description: 100 CLOTH in 1 BAG

NDC Product Information

Alcohol Wet Wipes with NDC 78122-102 is a a human over the counter drug product labeled by Wenzhou Guanshang Paper Co., Ltd. The generic name of Alcohol Wet Wipes is alcohol wipes. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Wenzhou Guanshang Paper 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.

Alcohol Wet 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 2.625 mL/1

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: Wenzhou Guanshang Paper Co., Ltd
Labeler Code: 78122
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: 06-01-2020 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 Wet Wipes Product Label Images

Alcohol Wet 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

Alcohol 75% v/v. Purpose: Antiseptic



When Using

Avoid using in eyes, wounds and other sensitive parts.If it gets into eyes accidentally, please wash it with plenty of water.

Do Not Use

Do not use in eyes, wounds and other sensitive parts.

Stop Use

Stop use if irritation and redness develop. If condition continues, consult your health care practitioner.

Keep Out Of Reach Of Children

Do not let children touch it.

Indications & Usage

Sterilization, killing intestinal carcinogenic bacteria, laboratory cocci, pathogenic yeast and common bacteria of hospital infection.This product is suitable for wiping hands, face, skin, etc.


Unfold towlette, wipe hands, discard after use.


For external use only.Flammable, please stay away from fire or heat.

Other Information

Please put it in a cool and dry place, avoid direct sunlight.

Inactive Ingredient


* Please review the disclaimer below.