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Certus Antiseptic Towelette

Medically reviewed on April 12, 2018

Dosage form: swab
Ingredients: BENZALKONIUM CHLORIDE 0.0013mL in 1mL
Labeler: Certus Medical, Inc.
NDC Code: 75990-5018

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.

Certus Antiseptic Towelette 210032 Drug Facts and Label

Drug Facts Box OTC Active Ingredient Section

Benzalkonium Chloride 0.13% w/w

Drug Facts Box OTC Purpose Section

First Aid Antiseptic

Drug Facts Box OTC Indications & Usage Section

First aid antiseptic to help prevent the risk of infection in minor cuts, scrapes and burns

Drug Facts Box OTC Warnings Section

For external use only

Drug Facts Box OTC Do Not Use Section

in the eyes or apply over large areas of the body

longer than 1 week unless directed by a doctor

Drug Facts Box OTC Ask Doctor Section

in case of deep or puncture wounds, animal bites,  or serious burns

Drug Facts Box OTC Stop Use Section

and ask a doctor if the condition persists or gets worse

Drug Facts Box OTC Keep Out Of Reach Of Children Section

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

Drug Facts Box OTC Dosage & Administration Section

clean the affected area

apply a small amount of this product on the area 1 to 3 times daily

may be covered with a sterile bandage when dry

Drug Facts Box OTC Inactive Ingredient Section

purified water, sodium bicarbonate

Certus Antiseptic Towelette 210032 pouch

210032.jpg  Certus Antiseptic Towelette  pouch 

CERTUS ANTISEPTIC TOWELETTE 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75990-5018
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE0.0013 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM BICARBONATE 
Packaging
#Item CodePackage Description
1NDC:75990-5018-31.4 mL in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/01/2011
Labeler - Certus Medical, Inc. (966433653)

 
Certus Medical, 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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