NDC 69842-084 Benzethonium Chloride And Dyclonine Hydrochloride

Liquid Bandage

NDC Product Code 69842-084

NDC CODE: 69842-084

Proprietary Name: Benzethonium Chloride And Dyclonine Hydrochloride 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: Liquid Bandage 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

  • 69842 - Cvs Pharmacy
    • 69842-084 - Benzethonium Chloride And Dyclonine Hydrochloride

NDC 69842-084-30

Package Description: 10 mL in 1 BOTTLE, WITH APPLICATOR

NDC Product Information

Benzethonium Chloride And Dyclonine Hydrochloride with NDC 69842-084 is a a human over the counter drug product labeled by Cvs Pharmacy. The generic name of Benzethonium Chloride And Dyclonine Hydrochloride is liquid bandage. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Cvs Pharmacy

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

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.

Benzethonium Chloride And Dyclonine Hydrochloride 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.

  • ALCOHOL (UNII: 3K9958V90M)
  • ACETONE (UNII: 1364PS73AF)

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: Cvs Pharmacy
Labeler Code: 69842
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: 06-01-2019 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’.

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Benzethonium Chloride And Dyclonine Hydrochloride Product Label Images

Benzethonium Chloride And Dyclonine Hydrochloride 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 Ingredients

Benzethonium chloride 0.2%Dyclonine hydrochloride 0.75%


First aid antisepticTopical analgesic


  • First aid to prevent bacterial contamination in minor cuts, scrapes and burnsfor the temporary relief of pain


For external use only.


Keep away from fire or flame.

Do Not Use

  • In the eyesover large areas of the bodylonger than 1 week unless directed by a doctor

Ask A Doctor Before Use If You Have

  • Deep or puncture woundsdeep cutsanimal bitesserious burns

When Using This Product

  • Avoid contact with eyes.

Stop Use And Consult A Doctor If

  • Condition persists or gets worsesymptoms persist for more than 7 days or clear up an occur again within a few daysinfection occurs

Keep Out Of Reach Of Children.

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


  • For adults and children 2 years of age and olderclean affected areaapply a small amount on the area 1 to 3 times daily and let drya second coating may be applied for extra protectionchildren under 2 years of age: consult a doctor

Other Information

  • Cap tightlystore between 20º to 25º C (68º to 77ºF)may temporarily sting upon applicationto remove, apply more Liquid Bandage and quickly wipe off

Inactive Ingredient

Acetone, amyl acetate, castor oil, ethyl acetate, nitrocellulose, SD alcohol 40


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