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BSafe Instant Foaming Hand Sanitizer

Medically reviewed on Dec 19, 2017

Dosage form: aerosol, foam
Ingredients: BENZALKONIUM CHLORIDE 1mg in 1000mL
Labeler: Med-Dev Corporation
NDC Code: 69348-100

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.

B’Safe Instant Foaming Hand Sanitizer with Conditioners

Active ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Uses
For hand sanitizing to decrease bacteria on the skin
Recommended for repeated use
Significantly reduces bacteria on hands between regular hand washing but not intended to replace regular hand washing.

Warnings

For External use only.

When using this product avoid contact with eyes and nose. In case of contact flush eyes with water.

Stop use and consult a doctor if irritation or redness develops.

Keep out of reach of children.

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

Directions

Pump small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands. Rub hands together briskly until dry.

Inactive ingredients

Purified Water, Glycerin, Dihydroxyethyl Cocamine Oxide, Dihydroxypropyl PEG-5 Linoleammonium Chloride, Glycereth-17 Cocoate, Cetrimonium Chloride, Laurtrimonium Chloride

Package/Label Principal Display Panel - Carton Label

B’Safe
Instant Foaming
Hand Sanitizer
with Conditioners

B’Safe    B’Soft    B’Sure

Alcohol Free
Odorless
Non Flammable

1000ml

Med-Dev Corporation
TekRidge Center, 50 Alberigi Dr., Suite 106, Jessup, PA 18434

570-383-6772

MADE IN THE USA

Carton Label

BSAFE INSTANT FOAMING HAND SANITIZER 
benzalkonium chloride aerosol, foam
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69348-100
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1 mg  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
GLYCERIN 
DIHYDROXYETHYL COCAMINE OXIDE 
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE 
GLYCERETH-17 COCOATE 
CETRIMONIUM CHLORIDE 
LAURTRIMONIUM CHLORIDE 
Packaging
#Item CodePackage Description
1NDC:69348-100-011000 mL in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E12/04/2014
Labeler - Med-Dev Corporation (053927573)
Establishment
NameAddressID/FEIOperations
Fragrance Manufacturing, Inc.793406000MANUFACTURE(69348-100)

 
Med-Dev Corporation

Further information

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

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