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Deb InstantFOAM Non-Alcohol PURE

Medically reviewed on Dec 21, 2017

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 0.13g in 100mL
Labeler: Deb USA, Inc.
NDC Code: 11084-001

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

BENZALKONIUM CHLORIDE, 0.13%   

Purpose

Antibacterial

Uses

for hand sanitizing 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 one shot to dry hands, rub into skin

no rinsing required

Inactive ingredients

ALOE BARBADENSIS LEAF JUICE, AQUA (WATER), COCAMIDOPROPYL BETAINE, LAURAMINE OXIDE, MAGNESIUM CHLORIDE, MAGNESIUM NITRATE, METHYLCHLOROISOTHIAZOLINONE, METHYLISOTHIAZOLINONE, PROPYLENE GLYCOL, TETRASODIUM EDTA

deb stoko

Deb InstantFOAM(R) Non-Alcohol PURE

Dye & Fragrance Free Hand Sanitizer

Antiseptico para manos en espuma - sin alcohol, sin colorante y sin perfume

SANITIZE

NON-ALCOHOL

DCN8901/1116

Deb USA, Inc. Charlotte,

NC 28217. 1-800-248-7190

www.debgroup.com

Made in USA

1 L

(33.8 fl oz)

DEB INSTANTFOAM NON-ALCOHOL PURE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF 
WATER 
COCAMIDOPROPYL BETAINE 
LAURAMINE OXIDE 
MAGNESIUM CHLORIDE 
MAGNESIUM NITRATE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
PROPYLENE GLYCOL 
EDETATE SODIUM 
Packaging
#Item CodePackage Description
1NDC:11084-001-0147 mL in 1 BOTTLE, PLASTIC
2NDC:11084-001-40400 mL in 1 BOTTLE, PLASTIC
3NDC:11084-001-271000 mL in 1 BOTTLE, PLASTIC
4NDC:11084-001-121200 mL in 1 BOTTLE, PLASTIC
5NDC:11084-001-991230000 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A09/07/2016
Labeler - Deb USA, Inc. (607378015)
Establishment
NameAddressID/FEIOperations
Deb USA, Inc.078805627manufacture(11084-001)
Establishment
NameAddressID/FEIOperations
Deb Worldwide Healthcare Inc.205662831repack(11084-001)

 
Deb USA, Inc.

Further information

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

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