Label: LIQUID BANDAGE- benzethonium chloride plus dyclonine hydrochloride liquid
- NDC Code(s): 56104-502-00
- Packager: Premier Brands of America Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 26, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
- Questions
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
LIQUID BANDAGE
benzethonium chloride plus dyclonine hydrochloride liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:56104-502 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) AMYL ACETATE (UNII: 92Q24NH7AS) CASTOR OIL (UNII: D5340Y2I9G) ETHYL ACETATE (UNII: 76845O8NMZ) PYROXYLIN (UNII: KYR8BR2X6O) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:56104-502-00 1 in 1 CARTON 09/11/2023 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 09/11/2023 Labeler - Premier Brands of America Inc. (117557458)