DEB MED ANTIMICROBIAL FOAMING HAND WASH FRAGRANCE FREE DYE FREE- 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, 0.70%

Purpose

Antimicrobial

Uses

For hand washing to reduce bacteria on the skin

Warnings

For external use only

When using this product avoid contact with eyes.

In case of eye contact, flush with water

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply foaming cleanser to hands

Rub hands together to spread lather

Wash for 15-20 seconds

Rinse and dry hands thoroughly

Inactive ingredients

Water, Propyl Alcohol, Butylene Glycol, Sodium Laureth Sulfate, Disodium Laureth Sulfosuccinate, Cocamidopropyl Betaine, Ethylhexylglycerin, Benzyl Alcohol, Phenoxyethanol, Polyglycerin-6, Citric Acid, DMDM Hydantoin, Cocamidopropyl PG-Dimonium Chloride Phosphate, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Tetrasodium EDTA, Allantoin, Methylchloroisothiazolinone, Methylisothiazolinone.

deb med Engineering Hand Hygiene Compliance

AntiMicrobial Foaming Hand Wash with Microhydration

Meets Protocol For Healthcare Personnel Handwash

400 mL

13.5 fl. oz.

Made in USA

www.debgroup.com

DMDF400ML

Fragrance Free Dye Free

Rev. 09-13

container label

DEB MED ANTIMICROBIAL FOAMING HAND WASH FRAGRANCE FREE DYE FREE 
triclosan liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:11084-266
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X) TRICLOSAN 7 mg  in 100 mL
Inactive Ingredients
Ingredient Name Strength
WATER (UNII: 059QF0KO0R)  
PROPYL ALCOHOL (UNII: 96F264O9SV)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)  
DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
POLYGLYCERIN-6 (UNII: M51422LRAM)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
DMDM HYDANTOIN (UNII: BYR0546TOW)  
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
EDETATE SODIUM (UNII: MP1J8420LU)  
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)  
ALLANTOIN (UNII: 344S277G0Z)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11084-266-40 400 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 09/15/2013
Labeler - Deb USA, Inc. (607378015)
Establishment
Name Address ID/FEI Business Operations
Deb USA, Inc. 607378015 manufacture(11084-266)

Revised: 9/2013
Document Id: d28978d9-c9ce-49c2-b903-658d59b02230
Set id: 5c67eba9-ca90-4ba5-9a39-714c7cf1bdfb
Version: 2
Effective Time: 20130912
 
Deb USA, Inc.