STOKO REFRESH- triclosan liquid

Stoko Refresh by

Drug Labeling and Warnings

Stoko Refresh by is a Otc medication manufactured, distributed, or labeled by Evonik Stockhausen, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Triclosan (0.5%)

Purpose

Antimicrobial hand wash

Use

Cleanse harmful bacteria and dirt from the skin.

Warning

• For external use only
• If swallowed, get medical help or contact a Poison Control Center right away
• Should solution enter eyes, flush immediately with water
  

• Keep out of reach of children
  

Directions

Place one pump in palm, add a little water and wash thoroughly. Rinse hands after washing.

Inactive Ingredients

Water, Sodium Cumenesulfonate, Sodium Laureth Sulfate, Propylene Glycol, Cocamidopropyl Betaime, Sodium Benzoate, Citric Acid, Fragrance, Yellow 6.

Questions?

800-334-0242 (Mon-Fri, 8am-5pm EST)

Principal Display Panel

Stoko

Refresh

Anti-Bacterial Foam

How To Install:

Align bottle in to dispenser. Press firmly into place

until pump clicks. Close cover. Press dispenser to

prime. To replace, push green tab up to release bottle.

Aligner la bouteille dans le distributeur

L'inserer fermement en place jusqu'a ce que la pompe emette

un clic. Fermer le couvercle. Appuyer sur le distributeur pour

rendre la pompe prete a distribuer le produit. Pour remplacer,

appuyer sur la languette verte afin de degager la bouteille.

Alinee la botella en el aplicador

Presionela firmemente en su lugar hasta que la bomba

haga "click". Cierre la cubierta. Presione el aplicador para

cebar la bomba. Para reemplazar, presione la pestana

verde para liberar la botella.

Should Solution Enter The Eyes

Flush Immediately With Water

Stoko Skin Care

Evonik Stockhausen, LLC

Greensboro, NC 27406

1-800-334-0242 I www.StokoSkinCare.com

Made in the USA

Stock#34969

Net contents: 1000 ml (33.82 fl. oz.)

INGREDIENTS AND APPEARANCE

STOKO REFRESH 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 64064-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Triclosan (UNII: 4NM5039Y5X) (Triclosan - UNII:4NM5039Y5X)	Triclosan	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Sodium Cumenesulfonate (UNII: 5798KA13PG)
Sodium Laureth Sulfate (UNII: BPV390UAP0)
Propylene Glycol (UNII: 6DC9Q167V3)
Cocamidopropyl Betaine (UNII: 5OCF3O11KX)
Sodium Benzoate (UNII: OJ245FE5EU)
Citric Acid Monohydrate (UNII: 2968PHW8QP)
FD&C Yellow No. 6 (UNII: H77VEI93A8)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 64064-101-01	1000 mL in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	03/01/2011

Labeler - Evonik Stockhausen, LLC (089906614)

Establishment
Name	Address	ID/FEI	Business Operations
Evonik Stockhausen, LLC		089906614	manufacture