CERTUS WASH TOWELETTE- benzalkonium chloride swab

Certus Wash Towelette by

Drug Labeling and Warnings

Certus Wash Towelette by is a Otc medication manufactured, distributed, or labeled by Certus Medical, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

fragrance, isopropyl alcohol, propylene glycol, purified water, sodium bicarbonate

Certus Wash Towelette 210033 pouch

210033.jpg  Certus Wash Towelette  pouch 

INGREDIENTS AND APPEARANCE

CERTUS WASH TOWELETTE 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75990-5028
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.0013 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75990-5028-3	1.4 mL in 1 POUCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/01/2011

Labeler - Certus Medical, Inc. (966433653)