LIQUID BANDAGE- benzethonium chloride and dyclonine hydrochloride liquid

Liquid Bandage by

Drug Labeling and Warnings

Liquid Bandage by is a Otc medication manufactured, distributed, or labeled by Wal-Mart Stores, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Benzethonium chloride 0.2%
Dyclonine hydrochloride 0.75%

Purpose

First aid antiseptic
Topical analgesic

Uses

• first aid to prevent bacteria contamination in minor cuts, scrapes and burns
• For the temporary relief of pain

Warnings

For external use only.

Flammable:

Keep away from fire or flame.

Do not use

• in the eyes
• over large areas of the body
• longer than 1 week unless directed by a doctor

Ask a doctor before use if you have

• deep puncture wounds
• deep cuts
• animal bites
• serious burns

When using this product

• avoid contact with eyes

Stop use and ask a doctor if

• conditions persists or gets worse
• symptoms persists for more than 7 days or clear up and occur again within a few days
• infection occurs

Keep out of reach of children.

If swallowed, get medical help or call a Poison Control Center right away.

Directions

• for adults and children 2 years of age and older
• Clean affected area
• apply a small amount on the area 1-3 times daily
• let dry
• a second coating may be applied for extra protection
• children under 2 years of age: consult a doctor

Other information

• cap bottle tightly
• store between 20° to 25°C (68° to 77°F)
• may temporarily sting upon application
• to remove, apply more liquid bandages and quickly wipe off

Inactive ingredients

acetone, amyl acetate, castor oil, ethyl acetate, nitrocellulose, SD slcohol 40

Questions

Call 1-888-287-1915

Principal Display Panel

Equate

Liquid

Bandage

Topical Analgesic & Antiseptic

Seals to Protect

• Helps prevent infection
• Invisible & Flexible
• Water Resistant
• Built-in applicator brush

0.3 FL OZ (9 mL)

INGREDIENTS AND APPEARANCE

LIQUID BANDAGE 
benzethonium chloride and dyclonine hydrochloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79903-485
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.06 mg  in 29.6 mL
DYCLONINE HYDROCHLORIDE (UNII: ZEC193879Q) (DYCLONINE - UNII:078A24Q30O)	DYCLONINE HYDROCHLORIDE	0.23 mg  in 29.6 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: 79903-485-30	29.6 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	01/31/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	01/12/2012

Labeler - Wal-Mart Stores, Inc. (051957769)