ANTIBACTERIAL HAND- triclosan liquid

Antibacterial Hand by

Drug Labeling and Warnings

Antibacterial Hand by is a Otc medication manufactured, distributed, or labeled by Walgreen Co, Vi-Jon. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient
Triclosan 0.15%

Purpose
Antibacterial

INDICATIONS & USAGE

Uses for handwashing to decrease bacteria on the skin

WARNINGS

Warnings
For external use only

When using this product do not get into eyes.  If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if irritation or redness develops

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions wet hands apply palmful to hands scrub thoroughly rinse

INACTIVE INGREDIENT

Inactive ingredients water, sodium laureth sulfate, sodium lauryl sulfate, cocamidopropyl betaine, sodium chloride, decyl glucoside, glycerin, PEG-18 glyceryl oleate/cocoate, fragrance, cocamide MEA,
DMDM hydantoin, tetrasodium EDTA, citric acid, yellow 5, red 4

SPL UNCLASSIFIED SECTION

This product is not manufactured or distributed by The Dial Corporation,
distributor of Dial Gold Antibacterial Soap

ADVERSE REACTIONS

DISTRIBUTED BY:  WALGREEN CO.
200 WILMOT RD, DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
walgreens.com

PRINCIPAL DISPLAY PANEL

Studio 35
LIQUID
ANTIBACTERIAL
HAND SOAP
With Moisturizers
Compare to Dial Gold
Antibacterial Soap
11.25 FL OZ
(332 mL)

INGREDIENTS AND APPEARANCE

ANTIBACTERIAL HAND 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-0243
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	0.15 kg  in 100 L

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-18 GLYCERYL OLEATE/COCOATE (UNII: VD2D270332)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
DMDM HYDANTOIN (UNII: BYR0546TOW)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
FD&C RED NO. 4 (UNII: X3W0AM1JLX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-0243-81	.332 L in 1 BOTTLE, PLASTIC
2	NDC: 0363-0243-97	1.89 L in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333A	04/04/2012

Labeler - Walgreen Co (008965063)

Registrant - Vi-Jon (088520668)

Establishment
Name	Address	ID/FEI	Business Operations
Vi-Jon		088520668	manufacture