NDC 67151-303 Wipes Plus

Benzalkonium Chloride

NDC Product Code 67151-303

NDC 67151-303-01

Package Description: 80 SWAB in 1 PACKAGE

NDC 67151-303-04

Package Description: 240 SWAB in 1 BOTTLE

NDC 67151-303-07

Package Description: 800 SWAB in 1 BOTTLE

NDC 67151-303-08

Package Description: 1200 SWAB in 1 BOTTLE

NDC 67151-303-09

Package Description: 1500 SWAB in 1 BOTTLE

NDC Product Information

Wipes Plus with NDC 67151-303 is a a human over the counter drug product labeled by Progressive Products, Llc. The generic name of Wipes Plus is benzalkonium chloride. The product's dosage form is swab and is administered via topical form.

Labeler Name: Progressive Products, Llc

Dosage Form: Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab 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.

Wipes Plus 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 .0062 g/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)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • ALOE VERA LEAF (UNII: ZY81Z83H0X)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • QUATERNIUM-15 (UNII: E40U03LEM0)
  • DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
  • .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

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: Progressive Products, Llc
Labeler Code: 67151
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: 09-04-2020 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.

Wipes Plus 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 sanitizing to decrease bacteria on the skin.Apply topically to the skin to help prevent cross contamination.Recommended for repeated use.Dries in seconds.

Warnings

  • For external use onlyMay irritate eyes

Otc - Keep Out Of Reach Of Children

Keep out of reach of children unless under adult supervision

Directions

  • Remove lid.Pull wipe from enter of roll and thread through opening lid. Do not push finger through oepning.Replace lid, pull wipe up, and then out at 45 angle.The next wipe dispenses automatically.Close lid to retain moisture.

Inactive Ingredients

Water, Propylene glycol,Disodium EDTA, Chloro-methyl-isothiazolinone and Methyl-isothizolinone, Potassium Sorbate, Quaternium-15,Aloe barbadensis Leaf Juice,Disodium Cocoamphodiacetate, Vitamin E Acetate, Polysorbate-20, Citric acid, Fragrance

* Please review the disclaimer below.