ACTIVE WIPES- benzalkonium chloride paste

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium chloride 0.13% w/w

PURPOSE

Antimicrobial

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

When using this product
do not use in or near eyes
discontinue use if irritation and redness develop

DOSAGE & ADMINISTRATION

wet hands thoroughly with wipe allow to dry without rinsing

INDICATIONS & USAGE

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

INACTIVE INGREDIENT

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ACTIVE WIPES 
benzalkonium chloride paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84323-008
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
CITRIC ACID (UNII: 2968PHW8QP)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
ALCOHOL (UNII: 3K9958V90M)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84323-008-01	1500 in 1 BAG	05/08/2026
1		3 g in 1 PACKET; 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)	05/08/2026

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