BENZALKONIUM CHLORIDE- first aid antiseptic foam aerosol, foam

Benzalkonium chloride by

Drug Labeling and Warnings

Benzalkonium chloride by is a Otc medication manufactured, distributed, or labeled by Target Corp, Consumer Product Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.13% w/w

Purpose

First aid antiseptic

Uses

first aid to help prevent the risk of infection in:

• minor cuts 
• scrapes 
• burns

Warnings

For external use only

Do not use

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

Ask a doctor before use if you have

deep or puncture wounds, animal bites or 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: do not use, consult a doctor

Inactive ingredients

water, poloxamer 188, sodium chloride, disodium EDTA, sodium hydroxide, Aloe barbadensis leaf juice, citric acid

ADVERSE REACTION

Dist. by Target Corp., Mpls., MN 55403

TM & ©2024 Target Brands, Inc.

Disclaimers

*This product is not manufactured or distributed by Kenvue Inc., distributor of Band-Aid ®Antiseptic Cleansing Foam for Kids.

**Tested on select bacteria commonly associated with minor cuts, scrapes and burns.

PRINCIPAL DISPLAY PANEL

Compare to Band-Aid ®Antiseptic Cleansing Foam for Kids*

First Aid Antiseptic Foam

For Kids

• Kills 99.99% of germs**
• For minor cuts, scrapes and burns

No Sting

Contains Aloe

up & up™

2.3 FL OZ (68 mL)

INGREDIENTS AND APPEARANCE

BENZALKONIUM CHLORIDE 
first aid antiseptic foam aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11673-681
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)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11673-681-23	68 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/11/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/11/2025

Labeler - Target Corp (006961700)

Registrant - Consumer Product Partners, LLC (119091520)

Establishment
Name	Address	ID/FEI	Business Operations
Consumer Product Partners, LLC		119091514	manufacture(11673-681)