Soo'AE Hand Sanitizing Wipes 20

SooAE HAND SANTIZING WIPES by

Drug Labeling and Warnings

SooAE HAND SANTIZING WIPES by is a Otc medication manufactured, distributed, or labeled by DKCOS CORP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SOOAE HAND SANTIZING WIPES- benzalkonium chloride cloth 
DKCOS CORP

----------

Soo'AE Hand Sanitizing Wipes 20

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antiseptic handwash

Uses

• For hand washing to decrease bacteria on the skin

Warnings

For external use only

Do not use

• If you are allergic to any of the ingredients

When using this product

• Do not get into eyes. If contact occurs, rinse thoroughly with water

Stop use and ask a doctor if

• Irritation or rash develops and continues for more than 72 hours

Keep out of reach of children

• Unless under adult supervision
• If swallowed, get medical help or contact a Poison Control Center right away

Directions

• Use entire wipe to thoroughly wipe hands, fingers, and wrists
• To sanitize, use multiple wipes
• Discard after single use
• Keep label closed to prevent moisture loss

Other information

• Read the directions and warning before use
• Avoid freezing and excessive heat

Inactive ingredients

Water (Aqua), Phenoxyethanol, Glycerin, Sodium Benzoate, Polysorbate 20, Disodium EDTA, Citric Acid, Tocopheryl Acetate

Questions or Comments?

• E-mail: cs@dkcos.com
• Call 1-212-484-2621

Distributed by

Dist. by dkcos
New York, NY 10001
www.sooaenewyork.com
www.dkcos.com

Package Label - Principal Display Panel

Soo'AE

HAND SANITIZING WIPES

KILLS 99.9% OF GERMS*

20 WIPES

WIPE SIZE 5.9 X 7.9 in (15 X 20 cm)

SOOAE HAND SANTIZING WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 74166-302
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 mg

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)	Â
PHENOXYETHANOL (UNII: HIE492ZZ3T)	Â
GLYCERIN (UNII: PDC6A3C0OX)	Â
SODIUM BENZOATE (UNII: OJ245FE5EU)	Â
WATER (UNII: 059QF0KO0R)	Â
POLYSORBATE 20 (UNII: 7T1F30V5YH)	Â
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	Â
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	Â

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 74166-302-20	20 in 1 POUCH; Type 0: Not a Combination Product	04/30/2020	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/30/2020	12/31/2024

Labeler - DKCOS CORP (114993964)

Revised: 12/2024

Document Id: 2a5e4474-e805-a08d-e063-6294a90a0fec

34390-5

Set id: f0fe988b-e2e0-df4b-e053-2995a90a115a

Version: 3

Effective Time: 20241231

Â