ACTIVE WIPES- benzalkonium chloride patch

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium chloride 0.13% w/w

PURPOSE

Antimicrobial

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

WARNINGS

For external use only

DOSAGE & ADMINISTRATION

to sanitize hands without requiring water or a rinse
kills 99.9% of most common germs

INDICATIONS & USAGE

wet hands thoroughly with wipe allow to dry without rinsing

INACTIVE INGREDIENT

Water, SD Alcohol 40, Phenoxyethanol, Decyl Glucoside, Potassium Sorbate, Sodium Benzoate, Disodium EDTA, Citric Acid, Aloe Barbadensis (Aloe) Leaf Extract, Fragrance

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACTIVE WIPES 
benzalkonium chloride patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84323-009
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 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84323-009-01	1500 in 1 BAG	05/22/2026
1		3 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/22/2026

Labeler - Zhejiang StarryApex Biotechnology Co.,Ltd. (449987211)