Deb Med Antimicrobial Foaming Hand Wash Fragrance Free Dye Free by Deb USA, Inc. / Deb Worldwide Healthcare, Inc. Drug Facts

Deb Med Antimicrobial Foaming Hand Wash Fragrance Free Dye Free by

Drug Labeling and Warnings

Deb Med Antimicrobial Foaming Hand Wash Fragrance Free Dye Free by is a Otc medication manufactured, distributed, or labeled by Deb USA, Inc., Deb Worldwide Healthcare, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

1L

33.8 fl oz

Made in USA

www.debgroup.com

DMAMDF1L

Fragrance Free Dye Free

Rev. 01-11

DEB MED ANTIMICROBIAL FOAMING HAND WASH FRAGRANCE FREE DYE FREE 
triclosan liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11084-066
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TRICLOSAN (UNII: 4NM5039Y5X) (TRICLOSAN - UNII:4NM5039Y5X)	TRICLOSAN	.70 mL  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: 11084-066-27	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	02/10/2011	12/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/10/2011	12/01/2019

Labeler - Deb USA, Inc. (607378015)

Establishment
Name	Address	ID/FEI	Business Operations
Deb USA, Inc.		078805627	manufacture(11084-066)

Establishment
Name	Address	ID/FEI	Business Operations
Deb Worldwide Healthcare, Inc.		205662831	manufacture(11084-066)

Revised: 11/2017

Document Id: 690adc1a-2cb0-4774-a2e9-6a4eeb5b9011

34390-5

Set id: 631d3323-a51a-4595-8a68-d93bebc10337

Version: 4

Effective Time: 20171107

 

Deb USA, Inc.