BENZALKONIUM CHLORIDE- hand sanitizing wipes cloth

Benzalkonium Chloride by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredients

Benzalkonium Chloride 0.13%

Purpose

Antiseptic

Uses

• For hand sanitizing to decrease bacteria on the skin
• Apply topically to the skin to help prevent cross contamination
• Recommended for repeated use
• Dries in seconds

Warnings

For external use only.

May irritate eyes.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children unless under adult supervision

Directions

• Remove lid
• Pull wipe from center of roll and thread through opening in lid

Do not push finger through opening

• Replace lid, pull wipe up, and then out 45º angle

The next wipe dispenses automatically

• Close lid to retain moisture

Inactive ingredient

Aloe Barbadensis Leaf Juice, Disodium EDTA, DMDM Hydantoin, Ethylparaben, Fragrance, Methylparaben, Phenoxyethanol, Polysorbate 20, Sodium Citrate, Water

Principal Display Panel

wipesplus

HAND SANITIZING

alcohol wipes

lemon scent

Kills 99.9% of germs

INGREDIENTS AND APPEARANCE

BENZALKONIUM CHLORIDE 
hand sanitizing wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67151-313
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
ETHYLPARABEN (UNII: 14255EXE39)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
DMDM HYDANTOIN (UNII: BYR0546TOW)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
METHYLPARABEN (UNII: A2I8C7HI9T)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67151-313-04	240 in 1 CANISTER	03/29/2022
1		1 mg in 1 CANISTER; Type 0: Not a Combination Product
2	NDC: 67151-313-09	1500 in 1 CANISTER	03/29/2022
2		1 mg in 1 CANISTER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/29/2022

Labeler - Progressive (127111792)