NDC 41546-019 Trade Mark Sanitizing Wipe

Trade Mark Sanitizing Wipe

NDC Product Code 41546-019

NDC CODE: 41546-019

Proprietary Name: Trade Mark Sanitizing Wipe What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Trade Mark Sanitizing Wipe What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 41546 - Zhejiang Huanghua Biological Technology Co., Ltd

NDC 41546-019-01

Package Description: 1 CLOTH in 1 PACKET

NDC Product Information

Trade Mark Sanitizing Wipe with NDC 41546-019 is a a human over the counter drug product labeled by Zhejiang Huanghua Biological Technology Co., Ltd. The generic name of Trade Mark Sanitizing Wipe is trade mark sanitizing wipe. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Zhejiang Huanghua Biological 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.

Trade Mark Sanitizing Wipe 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 3.93 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.

Product Labeler Information

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

Labeler Name: Zhejiang Huanghua Biological Technology Co., Ltd
Labeler Code: 41546
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: 12-11-2020 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.

Trade Mark Sanitizing Wipe Product Label Images

Trade Mark Sanitizing Wipe 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

Ethyl Alcohol 75%




For sanitizing to help reduce bacteria on the skin.


For external use only.Fammable. Keep away from heat or flame.

Otc - Do Not Use

On children less than two months of age

On open skin wounds

Otc - When Using

When using this product, keep out of eyes,ears, and mouth. ln case of contact with eyes, rinse thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if irritation orrash occurs.These may be signs of a serious condition.

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children. lf swallowed, get medical help or contacta poison control center right away.


Open packetPul out wipe

Thoroughly wipe to clean
Discard wipe properlyDiscard empty packageSupervise children under 6 years of age when using this product

Other Information

Store in a cool dry place away from heat,direct sunlight,or flames.Wipe is insoluble in water. Do not flush down the toilet. This product may discolor certain fabrics or surfaces.

Inactive Ingredient


* Please review the disclaimer below.