NDC 73030-020 Trip Wipes

Benzalkonium Chloride

NDC Product Code 73030-020

NDC Product Information

Trip Wipes with NDC 73030-020 is a a human over the counter drug product labeled by Detroit Wick. The generic name of Trip Wipes is benzalkonium chloride. The product's dosage form is swab and is administered via topical form.

Labeler Name: Detroit Wick

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.

Trip 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 .13 g/100g

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)
  • PHENOXYETHANOL (UNII: HIE492ZZ3T)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • POLYSORBATE 20 (UNII: 7T1F30V5YH)
  • ORANGE OIL (UNII: AKN3KSD11B)
  • CITRUS MAXIMA FRUIT RIND OIL (UNII: 8U3877WD44)
  • BERGAMOT OIL (UNII: 39W1PKE3JI)
  • LINALOOL, (+/-)- (UNII: D81QY6I88E)
  • ETHYLENE BRASSYLATE (UNII: 9A87HC7ROD)
  • CITRAL (UNII: T7EU0O9VPP)
  • CITRUS JAPONICA FRUIT (UNII: 8PS197OFKT)
  • HEXAMETHYLINDANOPYRAN (UNII: 14170060AT)

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: Detroit Wick
Labeler Code: 73030
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: 04-15-2019 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: 12-31-2020 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.

Trip Wipes Product Label Images

Trip 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

Antimicrobial

Uses

  • For hand sanitizing to decrease bacteria on the skinRecommended for repeated use

Warnings

For external use only

When Using This Product

Avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop Use And Ask A Doctor

If irritation or redness develops, or if condition persists for more than 72 hours.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Take wipe and rub thoroughly over all surfaces of both hands. Wet hands thoroughly with wiperub hands together briskly to dry withut wipingdispose of wipedo not flush

Other Information

Store in cool dry place

Inactive Ingredients

Purified Water, Phenoxyethanol, Potassium Sorbate, Sodium Benzoate, Citric Acid, Polysorbate 20, Citrus Aurantium Dulcis Oil, Citrus Grandis Peel Oil, Citrus Aurantium Bergamia Fruit Oil, Elettaria Cardamomum Miniscula Seed, Linolool, Ehylene Brassylate, Citral, Kumquat Base, Galaxolide

* Please review the disclaimer below.

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