NDC 77878-027 Wipe Out Antibacterial Liquid Hand Coconut Vanilla

Benzalkonium Chloride

NDC Product Code 77878-027

NDC CODE: 77878-027

Proprietary Name: Wipe Out Antibacterial Liquid Hand Coconut Vanilla 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: Benzalkonium Chloride 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

  • 77878 - Tzumi Innovations Llc
    • 77878-027 - Wipe Out Antibacterial Liquid Hand Coconut Vanilla

NDC 77878-027-01

Package Description: 221 mL in 1 BOTTLE

NDC Product Information

Wipe Out Antibacterial Liquid Hand Coconut Vanilla with NDC 77878-027 is a a human over the counter drug product labeled by Tzumi Innovations Llc. The generic name of Wipe Out Antibacterial Liquid Hand Coconut Vanilla is benzalkonium chloride. The product's dosage form is soap and is administered via topical form.

Labeler Name: Tzumi Innovations Llc

Dosage Form: Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.

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.

Wipe Out Antibacterial Liquid Hand Coconut Vanilla 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.


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.

  • D&C RED NO. 7 (UNII: ECW0LZ41X8)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
  • 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: Tzumi Innovations Llc
Labeler Code: 77878
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: 12-23-2020 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 - NO 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

* Please review the disclaimer below.

Wipe Out Antibacterial Liquid Hand Coconut Vanilla Product Label Images

Wipe Out Antibacterial Liquid Hand Coconut Vanilla 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(S)

Benzalkonium Chloride  0.13%




For hand washing to decrease bacteria on the skin


For external use only

Otc - When Using

When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water

Otc - Stop Use

Stop use and ask a doctor if irritation and redness develop, condition persists for more than 72 hours

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.


  • Wet hands Apply palmful to handsScrub thoroughly for at least 15 secondsRinse thoroughly and dry

Inactive Ingredients

Water, Cocamidopropyl dimethylamine oxide, Citric Acid, Fragrance, Kathon, Glycerin, Fatty acyl diethanol amine, Disodium EDTA, Hydroxyethyl Cellulose (250HHR), Red 7 (CI 16255), Yellow 5 (CI 19140)

* Please review the disclaimer below.