SOFT WIPES- benzalkonium chloride cloth

Soft wipes by

Drug Labeling and Warnings

Soft wipes by is a Otc medication manufactured, distributed, or labeled by Vi-Jon, Albaad. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic

Use

for handwashing to decrease bacteria on the skin

Warings

For External use only-hands

When using this product

• keep out of eyes.  In case of contact with eyes, flush thoroughly with water.
• avoid contact with broken skin

Stop use and ask a doctor if

skin irritation develops

Keep out of reach of children

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

Directions

• wipe hands thoroughly with product and allow to dry
• for children under 6, use only under adult supervison
• not recommended for children

Inactive ingredients

water, polysorbate 20, glycerin, phenoxyethanol, aloe barbadensis leaf juice, fragrance, methylparaben, tocopheryl acetate, tetrasodium EDTA, disodium cocoamphodiacetate, butylparaben, citric acid, ethylparaben, propylparaben

questions?

1-866 MY GERMX - 1-866-694-3769

Size information

30 Antibacterial wipes 5.9" x 7.9"

(15 cm x 20 cm)

Adverse Reactions

Distributed by 

Vi-Jon

8515 Page Ave.

St. Louis MO 63114

principal display panel

GREAT FOR ON-THE-GO

GERM-X

ANTIBACTERIAL HAND WIPES

ALCOHOL FREE

Quick + Easy!

Gentle formula for dirty

Hands and Messy Faces!

Effective at eliminating 99.99% of many common harmful germs and bacteria in as little as 15 secinds.

30 SOFT WIPES

INGREDIENTS AND APPEARANCE

SOFT WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11344-919
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 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
water (UNII: 059QF0KO0R)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
METHYLPARABEN (UNII: A2I8C7HI9T)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EDETATE SODIUM (UNII: MP1J8420LU)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
ETHYLPARABEN (UNII: 14255EXE39)
PROPYLPARABEN (UNII: Z8IX2SC1OH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11344-919-65	30 in 1 POUCH	11/13/1998
1		3.0 mL 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 not final	part333A	11/13/1998

Labeler - Vi-Jon (150931459)

Registrant - Vi-Jon (790752542)

Establishment
Name	Address	ID/FEI	Business Operations
Albaad		143406457	manufacture(11344-919)