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TopSani

Medically reviewed on December 1, 2017

Dosage form: liquid
Ingredients: BENZALKONIUM CHLORIDE 1.25mL in 1000mL
Labeler: United Promotions Inc.
NDC Code: 24439-321

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.

topsani
HAND SANITIZER + MOISTURIZER

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.125%

Purpose

Antimicrobial

Indications

For handwashing to decrease bacteria on the skin.

Warning

For external use only.

When using this product avoid contact with the eyes. Rinse with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

Keep out of reach of children. If swallowed get medical help or contact a poison control center right away.

Directions

Wet hands thoroughly with product and allow to dry without wiping.

Inactive Ingredients

Blue 1, Fragrance, Hydroxypropyl Methylcellulose, Polysorbate-20, SD Alcohol 40-B, Urea, Water

Questions or Comments?

Call 1-877-541-6055

Dist. by UPI, Atlanta, GA 30326 USA

PRINCIPAL DISPLAY PANEL - 56 mL Bottle Label

non-alcohol based

PronTech™
Technology

topsani
HAND SANITIZER + MOISTURIZER

Lasting Anti-Bacterial Protection

KILLS 99.999%
of microorganisms

all you
need is a
dimesize
drop

2 FL OZ (56 mL)

TOPSANI 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24439-321
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1.25 mL  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL 
FD&C BLUE NO. 1 
HYPROMELLOSES 
POLYSORBATE 20 
UREA 
WATER 
Product Characteristics
ColorBLUEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:24439-321-1056 mL in 1 BOTTLE, PLASTIC
2NDC:24439-321-11236 mL in 1 BOTTLE, PUMP
3NDC:24439-321-12946 mL in 1 BOTTLE, PLASTIC
4NDC:24439-321-13946 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333E11/01/2011
Labeler - United Promotions Inc. (796252054)

 
United Promotions Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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