Your browser does not support JavaScript! CHEMSTAR INSTANTFOAM NONALCOHOL SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [DEB USA, INC.]
DailyMed Logo Header image

Daily Med

Current Medication Information

Options

RxNorm Names

CHEMSTAR INSTANTFOAM NONALCOHOL SANITIZER (benzalkonium chloride) liquid
[Deb USA, Inc.]


Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL OTC monograph not final
NOTE: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 Label Sections

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

Water, Propylene Glycol, Aloe Barbadensis Leaf Juice, Cocamidopropyl Betaine, Lauramine Oxide, Tetrasodium EDTA, Fragrance, Citric Acid, Magnesium Nitrate, Methylchloroisothiazolinone, Magnesium Chloride, Methylisothiazolinone, Blue 1 (CI 42090), Red 33 (CI 17200)

Chemstar Non-Alcohol Foaming Hand Sanitizer

Chemstar

product label

CHEMSTAR INSTANTFOAM NONALCOHOL SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11084-111
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
PROPYLENE GLYCOL 
ALOE VERA LEAF 
COCAMIDOPROPYL BETAINE 
LAURAMINE OXIDE 
EDETATE SODIUM 
ANHYDROUS CITRIC ACID 
D&C RED NO. 33 
FD&C BLUE NO. 1 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
MAGNESIUM NITRATE 
MAGNESIUM CHLORIDE 
Packaging
#Item CodePackage Description
1NDC:11084-111-271000 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A12/01/2012
Labeler - Deb USA, Inc. (607378015)
Registrant - Deb USA, Inc. (607378015)
Establishment
NameAddressID/FEIBusiness Operations
Deb USA, Inc.607378015manufacture(11084-111)

Revised: 12/2012
Document Id: 05aff63d-a288-4740-8a79-7bf86b6f88c3
Set id: df27f94c-3a84-4f97-9f91-bcab05c2d057
Version: 6
Effective Time: 20121206
 
Deb USA, Inc.

Visit The National Library of Medicine Copyright, Privacy, Accessibility
U.S. National Library of Medicine, 8600 Rockville Pike, Bethesda, MD 20894
National Institutes of Health, Health & Human Services