NDC 41546-012 Alcohol Wipes

Alcohol Wipes

NDC Product Code 41546-012

NDC 41546-012-01

Package Description: 100 CLOTH in 1 BAG

NDC Product Information

Alcohol Wipes with NDC 41546-012 is a a human over the counter drug product labeled by Zhejiang Huanghua Biological Technology Co., Ltd. The generic name of Alcohol Wipes is alcohol wipes. The product's dosage form is cloth and is administered via extracorporeal 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.

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 288 mL/1001
  • BENZALKONIUM CHLORIDE .5 g/1001
  • METHYLISOTHIAZOLINONE .5 g/1001
  • PROPYLENE GLYCOL .5 g/1001
  • PHENOXYETHANOL .5 g/1001

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.

  • Extracorporeal - Administration outside of the body.
  • Extracorporeal - Administration outside of the body.

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: part333E 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: 10-26-2020 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

Dosage & Administration

Store between 15-30°C(59-86°F),avoid freezing and excessive heat above 40°C(104°F)

Inactive Ingredient

Pure water

Indications & Usage

1.Open cover and remove seal.

2.Pull out wipe corner from center of the roll.

3.Thread through hole in the cover.

4.Close lid after use to retain moisture.

Otc - Active Ingredient

AlcoholBenzalkamine2-methyl-4-isothiazoline-3-onepropylene glyco2-phenoxyethanol

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Otc - Purpose

Disinfection

Sterilization

No Rinseing

Warnings

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

* Please review the disclaimer below.