BENZALKONIUM CHLORIDE- antibacterial hand wipes cloth

Benzalkonium Chloride by

Drug Labeling and Warnings

Benzalkonium Chloride by is a Otc medication manufactured, distributed, or labeled by Target Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

• for hand sanitizing to decrease bacteria on the skin
• recommended for repeated use

Warnings

For external use only.

Do not use

if you are allergic to any of these ingredients.

When using this product

avoid contact with eyes. In case of contact, flush eyes with water.

Stop use and ask a doctor

if irritation or redness develops, or if condition persists for more than 72 hours.

Keep out of reach of children.

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

Directions

• adults and children 2 years and over: apply to hands; allow to dry without wiping.
• Children under 2 years: ask a doctor before use.
• To dispense: Peel back front label slowly. Remove wipes.
• To reseal: Firmly rub thumb over label. Dispose of wipe in trash. Do not flush.

Other information

• store below 95°F (35°C)
• keep closed tightly
• may discolor certain fabrics or surfaces.

Inactive ingredients

Water, Phenoxyethanol, Decyl Glucoside, Disodium EDTA, Sodium Benzoate, Potassium Sorbate, Vitamin E, Aloe Barbadensis Leaf Extract, Citric Acid, Fragrance

PRINCIPAL DISPLAY PANEL

antibacterial

hand wipes

plant-based wipes

dermatologist tested

hypoallergenic

25 HAND WIPES

5½ IN X 8 IN

40 HAND WIPES

5½ IN X 8 IN

72 HAND WIPES

5½ IN X 8 IN

INGREDIENTS AND APPEARANCE

BENZALKONIUM CHLORIDE 
antibacterial hand wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82442-250
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82442-250-40	40 in 1 CONTAINER; Type 0: Not a Combination Product	03/03/2023
2	NDC: 82442-250-72	72 in 1 CONTAINER; Type 0: Not a Combination Product	03/03/2023
3	NDC: 82442-250-25	25 in 1 CONTAINER; Type 0: Not a Combination Product	03/03/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/03/2023

Labeler - Target Corporation (006961700)

Registrant - Target Corporation (006961700)