Label: BENZETHONIUM CHLORIDE AND DYCLONINE HYDROCHLORIDE- liquid bandage liquid
- NDC Code(s): 82442-019-01
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 22, 2026
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Directions
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Other information
- cap bottle tightly
- wipe top of bottle clean after each use
- store between 20 0 to 25 0C ( 68 0 to 77 0F)
- may temporarily sting upon application
- to remove, apply more Liquid Bandage and quickly wipe off
- do not allow to come into contact with fabrics, floors, countertops, or other surfaces - will stain
- Inactive ingredients
- Questions
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
BENZETHONIUM CHLORIDE AND DYCLONINE HYDROCHLORIDE
liquid bandage liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82442-019 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 2 mg in 1 mL DYCLONINE HYDROCHLORIDE (UNII: ZEC193879Q) (DYCLONINE - UNII:078A24Q30O) DYCLONINE HYDROCHLORIDE 7.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength ACETONE (UNII: 1364PS73AF) CASTOR OIL (UNII: D5340Y2I9G) ETHYL ACETATE (UNII: 76845O8NMZ) PYROXYLIN (UNII: KYR8BR2X6O) ALCOHOL (UNII: 3K9958V90M) AMYL ACETATE (UNII: 92Q24NH7AS) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82442-019-01 1 in 1 CARTON 04/09/2025 1 29.6 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 04/09/2025 Labeler - Target Corporation (006961700)

