Label: PREMIER SOLUTIONS LIQUID BANDAGE- benzethonium chloride dyclonine hydrochloride liquid
- NDC Code(s): 56104-246-01
- Packager: Premier Brands of America, Inc.
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated January 25, 2023
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- Official Label (Printer Friendly)
- Active ingredients
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
Stop use and ask a doctor if
- conditions persists or gets worse
- infection occurs
- symptoms persist for more than 7 days or clear up and occue again within a few days
- Other information
- Inactive ingredients
- Principal Display Panel
INGREDIENTS AND APPEARANCE
PREMIER SOLUTIONS LIQUID BANDAGE
benzethonium chloride dyclonine hydrochloride liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:56104-246 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 10 mL DYCLONINE HYDROCHLORIDE (UNII: ZEC193879Q) (DYCLONINE - UNII:078A24Q30O) DYCLONINE HYDROCHLORIDE 0.75 mg in 10 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:56104-246-01 10 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 06/16/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 06/16/2022 Labeler - Premier Brands of America, Inc. (117557458)