STOKO GEL INSTANT HAND SANITIZER- ethyl alcohol liquid

Stoko Gel Instant Hand Sanitizer by

Drug Labeling and Warnings

Stoko Gel Instant Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Deb USA, Inc., Deb-STOKO USA, LLC, Aphena Pharma Solutions-Maryland LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Ethanol (62%)

Purpose

Hand Antiseptic

Uses

Hand antiseptic to decrease bacteria on the skin

Flammable

For external use only.

Avoid contact with eyes. In case of accidental eye contact, flush eyes thoroughly with water.

Stop use and ask a doctor if

Skin or eye irritation 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

Dispense an adequate amount (approx. 5 mL), rubbing over all surfaces of both hands for at least 15 seconds. Allow to dry without wiping.

Inactive Ingredients

Deionized Water, Isopropanol, Hydrogenated Starch Hydrolysate, Carbomer, THP Ethylenediamine, Fragrance.

PRINCIPAL DISPLAY PANEL

NDC: 11084-910-87
NPN 80023556
NET CONTENTS 67.64 FL OZ
CONTENU NET 2000 mL
STOCK NO. 00888
No. De STOCK 00888
2000ml
Made in U.S.A.
deb
Manufactured in U.S.A.
Fabrique aux E.-U.
Deb USA, Inc.
Charlotte, NC 28217
1-800-248-7190 | www.stokoskincare.com
Distributed by/Distribue par
Deb Canada
Waterford, ON N0E 1Y0
1-888-332-7627
ALL IN ONE: Bottle, Valve and Label
STOKO®
Gel
Instant Hand Sanitizer

INGREDIENTS AND APPEARANCE

STOKO GEL INSTANT HAND SANITIZER 
ethyl alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-910
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYL ALCOHOL (UNII: 96F264O9SV)
HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V)
CARBOMER 940 (UNII: 4Q93RCW27E)
EDETOL (UNII: Q4R969U9FR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-910-11	118.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2014
2	NDC: 11084-910-10	236.6 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2014
3	NDC: 11084-910-87	2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2014
4	NDC: 11084-910-68	10 mL in 1 POUCH; Type 0: Not a Combination Product	06/01/2014

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2014

Labeler - SC Johnson Professional USA, Inc. (607378015)

Registrant - SC Johnson Professional USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
Aphena Pharma Solutions-Maryland LLC		829739833	manufacture(11084-910)