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Povidone Iodine Solution First Aid Antiseptic

Dosage form: solution
Ingredients: POVIDONE-IODINE 10kg in 100L
Labeler: Vi Jon
NDC Code: 0869-0050

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.

Drug Facts

Active ingredeint
Povidone-iodine, 10%(equivalent to 1% available iodine)


Uses first aid to help prevent the risk of infection in minor cuts, scrapes and  burns

For external use only

Ask A doctor before use if you have
• deep or puncture wounds
• animal bites
• serious burns

When using this product
• do not get into eyes.  If contact occurs, rinse eyes thoroughly with water
• do not apply over large areas of the body
• do not use longer than 1 week unless directed by a doctor

Stop use and ask a doctor if
• condition persists or gets worse

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

• 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.  If bandaged, let dry first.

Other information
store at room temperature

Inactive ingredients citric acid, disodium phosphate, glycerin, nonoxynol-9, purified water, sodium hydroxide

This product is not manufactured or distributed by the Purdue Frederick Company, distributor of Betadine

NDC 0896-0050-34  
Solution, 10%
Soluciond de povidona yodada. 10%
First Aid Antiseptic
Antisepito para primeros auxilios
Kills Germs in Monor, Burns, Cuts and Scrapes
Compare to Active Ingredient of Betadine
8 FL OZ (237 mL)

povidone-iodine solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0869-0050
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:0869-0050-34.2 L in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333E05/07/2009
Labeler - Vi Jon (790752542)
Registrant - Vi Jon (790752542)
Vi Jon790752542manufacture

Revised: 09/2010
Vi Jon

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.