NDC 79021-003 Antibacterial Wet Wipes

Benzalkonium Chloride

NDC Product Code 79021-003

NDC 79021-003-15

Package Description: 15 PATCH in 1 POUCH > 1.5 mL in 1 PATCH

NDC Product Information

Antibacterial Wet Wipes with NDC 79021-003 is a a human over the counter drug product labeled by Positive Promotions Inc.. The generic name of Antibacterial Wet Wipes is benzalkonium chloride. The product's dosage form is cloth and is administered via topical form.

Labeler Name: Positive Promotions Inc.

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.

Antibacterial 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.

  • BENZALKONIUM CHLORIDE 1.3 mg/mL

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)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • BENZOIC ACID (UNII: 8SKN0B0MIM)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • SODIUM CITRATE (UNII: 1Q73Q2JULR)

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: Positive Promotions Inc.
Labeler Code: 79021
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: 10-01-2020 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.

Antibacterial Wet Wipes Product Label Images

Antibacterial 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

Benzalkonium Chloride (0.13%)

Purpose

Antiseptic

Uses

  • For hand-washing to decrease bacteria on skin

Warnings

Flammable. Keep away from heat and flame.For External use only.

Do Not Use

In eyes. In case of contact, rinse thoroughly with water.

Stop Use & Ask Doctor

If rash/redness or irritation appears/develops and persist for more than 72 hours.

Keep Out Of Reach From Children

Except under adult supervision. If swallowed, get medical help or contact a Poison Control Center

Directions

  • Slowly peel back label and use one wipe. Reseal, keep closed to prevent evaporation.Thoroughly wipe hands, allow to dry out rinsing.Discard after single use

Other Information

  • Do not flush down toilet.Keep away from sunlight. Store at room temperature 20°-25°Celsius (68°-77° Fahrenheit)May discolor certain fabrics

Inactive Ingredients

Aqua, Glycerin, Phenoxyethanol, Benzoic Acid, Polysorbate 20, Aloe Barbadensis Leaf Juice, Sodium Citrate

* Please review the disclaimer below.