Label: BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE- liquid bandage liquid
- NDC Code(s): 63868-045-03
- Packager: Chain Drug Marketing Association
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 11, 2024
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
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Warnings
For external use only.
Do not use
- in the eyes
- over large areas of the body
- longer than 1 week unless directed by a doctor
- on infected areas or wounds that are draining
- with other first aid products such as lotions and creams
- over sutures
- on mucous membranes
Ask a doctor before use if you have
- deep puncture wounds
- deep cuts
- animal bites
- serious bleeding
- diabetes
- poor circulation
- serious burns
- Directions
- Other information
- Inactive ingredients
- Questions
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Principal Display Panel
Quality Choice
For Small Cuts & Wounds
Liquid Bandage
Antiseptic to Help Prevent Infection
Invisible | Flexible | Waterproof | Easy to use
Use Liquid Bandage For:
Blisters, chapped & cracked finger tips, hangnails, paper cuts, shaving nicks, & help in preventing the formulation of calluses.
Also Used By:
Bowlers, dancers, fishermen, golfers, hikers, musicians, runners, and tennis players
0.3 FL OZ. (9 mL)
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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:63868-045 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:63868-045-03 9 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 12/19/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 12/19/2017 Labeler - Chain Drug Marketing Association (011920774)