STOKO GEL INSTANT HAND SANITIZER- ethyl alcohol liquid 
SC Johnson Professional USA, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

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.

pn10088806 - Stoko Gel 2L.jpg

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

pn10088806 - Stoko Gel 2L.jpg

STOKO GEL INSTANT HAND SANITIZER 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-910
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
PROPYL ALCOHOL (UNII: 96F264O9SV)  
HYDROGENATED STARCH HYDROLYSATE (UNII: 27F77DSJ5V)  
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)  
EDETOL (UNII: Q4R969U9FR)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-910-11118.5 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/201412/31/2022
2NDC:11084-910-10236.6 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/201412/31/2022
3NDC:11084-910-872000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/201412/31/2022
4NDC:11084-910-6810 mL in 1 POUCH; Type 0: Not a Combination Product06/01/201412/31/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/01/201412/31/2022
Labeler - SC Johnson Professional USA, Inc. (607378015)
Registrant - SC Johnson Professional USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
Aphena Pharma Solutions-Maryland LLC829739833manufacture(11084-910)

Revised: 12/2022
Document Id: 74e09893-f46c-430e-b5d7-71d963f18158
Set id: c27618d3-931b-46e7-9cfd-9854059216aa
Version: 4
Effective Time: 20221220
 
SC Johnson Professional USA, Inc.