Label: BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE- liquid bandage liquid
- NDC Code(s): 37808-512-03
- Packager: HEB
- 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 23, 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
Ask a doctor before use if you have
- deep puncture wounds
- deep cuts
- animal bites
- serious bleeding
- poor circulation
- serious burns
When using this product
- do not sotre at temperaure above 120 oF
Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.
- Other information
- Inactive ingredients
Principle Display Panel
Topical Analgesic and
Antiseptic to Help Prevent Infection
For Small Cuts and Wounds
Use liquid bandage for blisters, chapped and cracked fingertips, hangnails, paper cuts, shaving nicks and to help in prevent the formation of calluses.
Used by bowlers, dancers, fishermen, golfers, hikers, musicians, runners, and tennis players.
- Easy to Use
0.3 FL OZ (9 mL)
INGREDIENTS AND APPEARANCE
BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE
liquid bandage liquid
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37808-512 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:37808-512-03 9 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 12/22/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 12/22/2017 Labeler - HEB (007924756)