ESTESOL GOLD- triclosan liquid 
Deb 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

Triclosan (0.5%)

Purpose

Antimicrobial hand wash

Uses

Cleanse harmful bacteria and dirt from the skin.

Warnings

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

Aqua (Water), Sodium Cumenesulfonate, Sodium Laureth Sulfate, Propylene Glycol, Cocamidopropyl Betaine, Hydroxypropyl Guar, Disodium EDTA, Parfum (Fragrance), 2-Bromo-2-Nitropropane-1,3-Diol, Yellow 6 (CI 15985).

NDC 11084-924-87

STOKO®
2000 ml
Net Contents: 67.64 fl.oz.
Stock #pn98330506
SKIN
CLEANSING
Estesol® gold
handwash
antibacterial hand cleanser
limpiador de manos antibacterial
savon antimicrobien pour les mains
Deb USA, Inc.
Charlotte, NC 28217
Phone + 1 800-248-7190
www.stokoskincare.com
deb

pn98330506 - pn80036500 - Estesol Gold

ESTESOL GOLD 
triclosan liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-924
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
SODIUM CUMENESULFONATE (UNII: 5798KA13PG)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
HYDROXYPROPYL GUAR (2500-4500 MPA.S AT 1%) (UNII: 3A1I7376TC)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
BRONOPOL (UNII: 6PU1E16C9W)  
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11084-924-872000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product06/01/201408/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/01/201408/01/2020
Labeler - Deb USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
Deb-STOKO USA, LLC055861874manufacture(11084-924)

Revised: 12/2017
Document Id: 3e3217ca-afe5-4672-ba2c-ba5fdbcf6dcb
Set id: d666658e-371d-437d-a9ac-ff01b4ada362
Version: 2
Effective Time: 20171222
 
Deb USA, Inc.