BENZALKONIUM CHLORIDE- dual action antimicrobial wipes cloth

Benzalkonium Chloride by

Drug Labeling and Warnings

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

Drug Details [pdf]

Active ingredient

Benzalkonium Chloride 0.13%

Purpose

Antimicrobial

Uses

For had washing to decrease bacteria on the skin. Recommended for repeated use.

Warnings

For external use only. Do not use over large areas of the bosy or if you are allergic to any of these ingredients.

When using this product

avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor

if irritation or redness develops and persists for more than 72 hours.

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• To use, peel back label, pull out wipe and firmly reseal label to maintain package moisture. Do not remove label.
• Unfold cloth and rub thoroughly over all surfaces of both hands. Use only once and throw away. After cleansing, dispose of wipe in a trash receptacle. Rub hands together briskly to dry.

Inactive ingredients

water, phenoxyethanol, decyl glucoside, potassium sorbate, sodium benzoate, disodium EDTA, citric acid, aloe barbadensis (aloe) leaf extract, fragrance.

Principal Display Panel

Dual Action

antibacterial wipes

150 cleaning wipes

7 in x 6 in (17.8 cm x 15.24 cm)

Gentle skin cleansers

No Rinse

*Kills 99.9% of germs that may cause illness including E. Coli and MRSA in just 15 seconds

Non-Alcohol Based Formula

Skin Moisturizing

Cleans & Refreshes

Fresh Scent

INGREDIENTS AND APPEARANCE

BENZALKONIUM CHLORIDE 
dual action antimicrobial wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73062-401
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

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
WATER (UNII: 059QF0KO0R)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
SODIUM BENZOATE (UNII: OJ245FE5EU)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73062-401-01	150 in 1 POUCH; Type 0: Not a Combination Product	10/26/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/26/2021

Labeler - Avro Enterprises LLC (804030166)