FOAMING HAND WASH ANTIBACTERIAL- triclosan liquid 
Target Corporation

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 Ingredients

Triclosan 0.6%

Purpose

Antibacterial

Use

Uses for hand washing to decrease bacteria on the skin

Warnings

Warnings

For external use only-hands only

When using this product

When using this product

Stop use and ask a doctor

Stop use and ask a doctor if irritation or redness develops

Keep out or reach of children

Keep out or freach of children except under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions

Inactive ingredients

Inactive ingredients water, sodium laureth sulfate, glycerin, cocamidopropyl betaine, ammonium xylenesulfonate, fragrance, disodium phosphate, citric acid, benzyl alcohol, red 4, yellow 5

Questions

Questions? Call 1-800-910-6874

Adverse reactions

Distributed by Target Corporation

Minneapolis, MN 55403

Made in U.S.A.

Target Brands, Inc.

All Rights Reserved Shop Target.com

Principal display panel

foaming hand wash

antibacterial

gently cleans hand

refill for foaming soap dispensers

Loaded Lather

up + up

50 FL OZ (1.4 L)

image description

FOAMING HAND WASH ANTIBACTERIAL 
triclosan liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-383
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 6 mg  in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
GLYCERIN (UNII: PDC6A3C0OX)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM)  
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11673-383-03 1478 mL in 1 BOTTLE, PUMP
2 NDC:11673-383-96 .221 mL in 1 PACKAGE
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 03/19/1993
Labeler - Target Corporation (006961700)
Registrant - Vi-Jon (790752542)
Establishment
Name Address ID/FEI Business Operations
Vi-Jon 088520668 manufacture(11673-383)

Revised: 10/2012
Document Id: 32c2012e-6950-432d-b329-de438fb525b5
Set id: dff095c3-e2bb-4065-b344-6c23be0bee8a
Version: 1
Effective Time: 20121002
 
Target Corporation