BAND AID ANTISEPTIC CLEANSING- benzalkonium chloride aerosol, foam

Band Aid Antiseptic Cleansing by

Drug Labeling and Warnings

Band Aid Antiseptic Cleansing by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

Active ingredient

Benzalkonium Cl (0.13%)

Purposes

First aid antiseptic

Use

first aid to help prevent infection in minor: · cuts · scrapes · burns

Warnings

• For external use only.

Do not use · in the eyes · over large area of the body · longer than 1 week

• Ask a doctor before use if you have · deep or puncture wounds · animal bites · serious burns

• Stop use and ask a doctor if the condition persists or gets worse

Keep out of reach of children.

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

Directions

adults and children 2 years of age and older:

clean the affected area
apply a small amount of this product on the area 1 to 3 times daily
may be covered with a sterile bandage
if bandaged, let dry first

children under 2 years of age: consult a doctor

Other information

protect from freezing

Inactive ingredients

Water, Poloxamer 188, Sodium Chloride, Disodium EDTA, Sodium Hydroxide, Aloe Barbadensis Leaf Juice, Citric Acid

Questions?

call 800-526-3967 or 215-273-8755 (collect).

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Distributed by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 68 mL Bottle

BAND-AID®

BRAND OF FIRST AID PRODUCTS

Johnson & Johnson

ANTISEPTIC

CLEANISING

FOAM

FIRST AID ANTIBIOTIC

Kids

Kills 99.99% of germs*

to prevent infection

No sting

Contains aloe

For minor cuts,

scrapes & burns

2.3 FL OZ (68mL)

INGREDIENTS AND APPEARANCE

BAND AID ANTISEPTIC CLEANSING 
benzalkonium chloride aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69968-0728
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
POLOXAMER 188 (UNII: LQA7B6G8JG)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69968-0728-1	68 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/29/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/29/2021

Labeler - Johnson & Johnson Consumer Inc. (118772437)