Label: BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE- liquid bandage liquid
- NDC Code(s): 68016-615-00
- Packager: Chain Drug Consortium, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 25, 2023
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- Active ingredients
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Liquid Bandage
FOR SMALL CUTS & WOUNDS
Topical analgesic and antiseptic to help prevent infection
Antiseptic formula dries quickly to form an invisible protective cover that is flexible
0.3 FL OZ (9mL)
Use Liquid Bandage for:
blisters, chapped and cracked finger tips, hangnails, paper cuts, shaving nicks and help in preventing the formation of calluses.
Great for:
athletes, active lifestyles, outdoor enthusiasts and musicians.
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INGREDIENTS AND APPEARANCE
BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE
liquid bandage liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-615 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE 0.2 mg in 9 mL DYCLONINE HYDROCHLORIDE (UNII: ZEC193879Q) (DYCLONINE - UNII:078A24Q30O) DYCLONINE HYDROCHLORIDE 0.75 mg in 9 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:68016-615-00 9 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 12/07/2005 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/07/2005 Labeler - Chain Drug Consortium, LLC (101668460)