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Refresh AntiBac Foam by Deb USA, Inc.

Medically reviewed on Dec 20, 2017

Dosage form: liquid
Ingredients: TRICLOSAN 3g in 1L
Labeler: Deb USA, Inc.
NDC Code: 11084-100

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.

Drug Facts

Active ingredient

TRICLOSAN, 0.30%

Purpose

Antibacterial

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 dry hands

rub hands together to spread lather

wash for 15-20 seconds

rinse and dry hands thoroughly

Inactive ingredients

AQUA (WATER), SODIUM LAURETH SULFATE, PROPYLENE GLYCOL, PEG-7 GLYCERYL COCOATE, GLYCERIN, COCAMIDOPROPYL BETAINE,
2-BROMO-2-NITROPROPANE-1,3-DIOL, PARFUM (FRAGRANCE), CITRIC ACID, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, GREEN 5 (CI 61570), YELLOW 5 (CI 19140)

deb stoko

Refresh

AntiBac FOAM

EN Pleasantly Perfumed Antibacterial Foam Handwash

ES Espuma antibacteriana y perfumada para higiene de manos

ANTIBACTERIAL

deb

Made in USA

Deb USA, Inc.

Charlotte, NC 28217

1-800-248-7190

www.debgroup.com

1 L

33.8 fl oz

DCN9019/0315

REFRESH ANTIBAC FOAM 
triclosan liquid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-100
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TRICLOSAN (TRICLOSAN) TRICLOSAN3 g  in 1 L
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURETH SULFATE 
PROPYLENE GLYCOL 
COCAMIDOPROPYL BETAINE 
CITRIC ACID MONOHYDRATE 
D&C GREEN NO. 5 
FD&C YELLOW NO. 5 
PEG-7 GLYCERYL COCOATE 
GLYCERIN 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
BRONOPOL 
Packaging
#Item CodePackage Description
1NDC:11084-100-400.4 L in 1 BOTTLE, PLASTIC
2NDC:11084-100-271 L in 1 BOTTLE, PLASTIC
3NDC:11084-100-121.2 L in 1 BOTTLE, PLASTIC
4NDC:11084-100-202 L in 1 BOTTLE, PLASTIC
5NDC:11084-100-991230 L in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
6NDC:11084-100-061.6 L in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/15/201508/01/2020
Labeler - Deb USA, Inc. (607378015)
Establishment
NameAddressID/FEIOperations
Deb USA, Inc.078805627manufacture(11084-100)
Establishment
NameAddressID/FEIOperations
Deb Worldwide Healthcare Inc.205662831repack(11084-100)

 
Deb USA, Inc.

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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