BENZALKONIUM CHLORIDE- sanitizing hand wipes cloth

Benzalkonium Chloride by

Drug Labeling and Warnings

Benzalkonium Chloride by is a Otc medication manufactured, distributed, or labeled by ALO NEW YORK LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

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 the 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 fron label slowly. Remove wipes.
• To reseal: Firmly rub thumb over label. Dispose of wipe in trash. Do not flush.

Other information

store below 95

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

Inactive ingredients

Purified Water, Decyl Glucoside, Aloe Barbadensis (Aloe) Leaf Extract, Phenoxyethanol, Citric Acid, Sodium Benzoate, Potassium Sorbate, Eucalyptus Globulus Oil, Mentha Piperita (Peppermint) Oil.

Principal Display Panel

ALO

20 Skin-Softening Sanitizing Hand Wipes

ALO

20 Individually Wrapped Sanitizing Hand Wipes

INGREDIENTS AND APPEARANCE

BENZALKONIUM CHLORIDE 
sanitizing hand wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82355-550
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0013 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
MENTHA PIPERITA (UNII: 79M2M2UDA9)
SODIUM BENZOATE (UNII: OJ245FE5EU)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
EUCALYPTUS GLOBULUS WHOLE (UNII: SI1P2XF3M3)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82355-550-02	20 in 1 PACKAGE	12/21/2021
1		1 mg in 1 PACKAGE; Type 0: Not a Combination Product
2	NDC: 82355-550-01	20 in 1 PACKAGE	12/21/2021
2		1 mg in 1 PACKAGE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	12/21/2021

Labeler - ALO NEW YORK LLC (110122374)