FIRST AID ANTISEPTIC WIPES (benzalkonium chloride- 0.13% cloth

First Aid Antiseptic Wipes by

Drug Labeling and Warnings

First Aid Antiseptic Wipes by is a Otc medication manufactured, distributed, or labeled by Walgreen CO, Vi-Jon, LLC, Albaad. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredients

Benalkonium chloride (0.13%)

Purpose

First Aid Antiseptic

Use

first aid to help prevent the rist of infection in minor cuts, scrapes, and burns

Warnings

For external use only

Do Not Use

in the eyes or apply over large areas of the body.

In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor.

Stop use and ask a doctor if

the condition persists or gets worse.  Do not use longer than 1 week unless directed by a doctor.

Keep out of reach of children.

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

Directions:

• clean the affected area
• apply a small amount of this product on the area 1 to 3 times daily
• may be covered with a sterile bandage
• if bandaged, let dry first

Inactive ingredients

water, glycerin, sodium cocoamphoacetate,  Aloe barbadensis leaf juice, tocopheryl acetate, fragrance, polysorbate 20, tetrasodium EDTA, phenoxyethanol, methylparaben, ethylparaben, potassium sorbate, sodium benzoate, sodium hydroxide, citric acid

adverse reactions

Walgreens Pharmacist Survey Study, November 2014

Questions or comments? 1-800-925-4733

DISTRIBUTED BY: WALGREEN CO.

200 WILMOT RD., DEERFIELD, IL 60015

100% SATISFACTION GUARANTEED

walgreens.com  2016 Walgreen Co.

MADE IN ISRAEL

952.000/952AA

PRINCIPAL DISPLAY PANEL

NEW

Well at

Walgreens

WALGREENS  PHARAMACIST RECOMMENDED

FIRST AID

Antiseptic 

Wipes

Benzalkonium chloride

• Antiseptic Cleansing Agent
• Helps reduce the risk of infection in minor cuts, scrapes and burns

20 WIPES

5.5 IN X 7.8 IN (140 mm x 200 mm)

INGREDIENTS AND APPEARANCE

FIRST AID ANTISEPTIC WIPES 
benzalkonium chloride (0.13%) cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0589
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	.0013 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM COCOAMPHOACETATE (UNII: W7Q5E87674)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
EDETATE SODIUM (UNII: MP1J8420LU)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLPARABEN (UNII: A2I8C7HI9T)
ETHYLPARABEN (UNII: 14255EXE39)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0589-01	20 in 1 CARTON	02/08/2017
1		1 mg in 1 PACKET; Type 1: Convenience Kit of Co-Package

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/08/2017

Labeler - Walgreen CO (008965063)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Albaad		143406457	manufacture(0363-0589)