NDC 75543-101 Alcohol Wipes

Alcohol Wipes

NDC Product Code 75543-101

NDC 75543-101-15

Package Description: 50 PATCH in 1 PACKAGE > 1 U in 1 PATCH (75543-101-01)

NDC Product Information

Alcohol Wipes with NDC 75543-101 is a a human over the counter drug product labeled by Fujian Yifa Healthcare Products Co., Ltd.. The generic name of Alcohol Wipes is alcohol wipes. The product's dosage form is patch and is administered via topical form.

Labeler Name: Fujian Yifa Healthcare Products Co., Ltd.

Dosage Form: Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.

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 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 15 U/100U

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: Fujian Yifa Healthcare Products Co., Ltd.
Labeler Code: 75543
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: 05-05-2020 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 Wipes Product Label Images

Alcohol 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

Benzalkonium Chloride, 0.15% w/w;Didecyldimonium Chloride, 0.2% w/w; Ethanol Alcohol, 15% w/w.

Inactive Ingredient

Phenoxyethanol, Propylene Glycol, Glycerin, Water.



When Using

Skin’s cleaning care, Article surface’s cleaning and maintenance.

Do Not Use

  • On children less than 2 months of ageon open skin wounds

Stop Use

Discontinue use if allergic reactions occur.

Keep Out Of Reach Of Children

Keep out of reach of children.

Indications & Usage

Skin’s cleaning care, Article surface’s cleaning and maintenance. Remove seal, pull out sheet and wipe skin or articles.(For external use only)

Dosage & Administration

Use it as needed, after following the usage instructions. For external use only.


This product is disposable and should not be reused. Check whether the package is in good condition before use. If the package is found to be untidy, it is not suitable for use.

* Please review the disclaimer below.