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Povidone-Iodine by Qualitest Pharmaceuticals

Dosage form: ointment
Ingredients: POVIDONE-IODINE 1g in 100g
Labeler: Qualitest Pharmaceuticals
NDC Code: 0603-0599

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.

Povidone-Iodine Ointment 10%
Maximum Strength

Active ingredient

Povidone-iodine 10% - equal to 1% available iodine


First aid antiseptic


first aid to help prevent infection in minor:

  • cuts
  • scrapes
  • burns


For external use only

Do not use
  • if you are sensitive to iodine or other product ingredients
  • in the eyes
  • for longer than one week unless directed by a doctor
  • over large areas of the body

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

Stop use and ask a doctor if
  • redness, irritation, swelling or pain continues or increases
  • infection occurs

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

Other information
  • avoid storing at excessive heat
  • lot number and expiration date: see crimp of tube or box
  • to open: unscrew cap, use pointed end on cap to puncture seal

You may report serious side effects to: 130 Vintage Drive, Huntsville, AL 35811.

Inactive ingredients

polyethylene glycols

Made in the USA
for Qualitest Pharmaceuticals
Huntsville, AL 35811

Rev. 5/15 R4
8280780 0599

povidone-iodine ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0603-0599
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:0603-0599-501 TUBE in 1 CARTON
128.4 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart333A08/01/199703/15/2018
Labeler - Qualitest Pharmaceuticals (011103059)
Vintage Pharmaceuticals-Huntsville825839835MANUFACTURE(0603-0599)

Revised: 08/2015
Qualitest Pharmaceuticals

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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.