BENZALKONIUM CHLORIDE- antibacterial hand wipes cloth 
Target Corporation

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.

----------

Antibacterial Hand Wipes

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

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

Other information

Inactive ingredients

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

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

254072

BENZALKONIUM CHLORIDE 
antibacterial hand wipes cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82442-250
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82442-250-4040 in 1 CONTAINER; Type 0: Not a Combination Product03/03/2023
2NDC:82442-250-7272 in 1 CONTAINER; Type 0: Not a Combination Product03/03/2023
3NDC:82442-250-2525 in 1 CONTAINER; Type 0: Not a Combination Product03/03/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/03/2023
Labeler - Target Corporation (006961700)
Registrant - Target Corporation (006961700)

Revised: 3/2023
Document Id: f604c684-8550-b7fe-e053-2a95a90a1a2c
Set id: f6037707-c6bb-11a0-e053-2995a90acce8
Version: 2
Effective Time: 20230303
 
Target Corporation