ESTESOL GOLD- triclosan liquid

Estesol Gold by

Drug Labeling and Warnings

Estesol Gold by is a Otc medication manufactured, distributed, or labeled by Deb USA, Inc., Deb-STOKO USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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).

PRINCIPAL DISPLAY PANEL

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

INGREDIENTS AND APPEARANCE

ESTESOL GOLD 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-924
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)
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11084-924-87	2000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	06/01/2014	08/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2014	08/01/2020

Labeler - Deb USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
Deb-STOKO USA, LLC		055861874	manufacture(11084-924)