Dosage form: solution
Ingredients: Povidone-Iodine 8mL in 100mL
Labeler: Dukal Corporation
NDC Code: 65517-0028
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 USP 7.5%
Antiseptic skin preparation
For external use only
- Do not use if allergic to iodine
- Stop use and ask a doctor if redness, irritation, swelling, or pain persists or increases
- Infection occurs
- Injuries are deep or puncture wounds or serious burns.
- Keep out of reach of children
- In case of accidental ingestion, seek professional assistance or consult a Poison Control Center immediately.
Clean the treatment area
- Apply a small amount of this product on the treatment area 1-3 times daily
- May be covered with a sterile bandage; if bandaged, let dry first.
0.75% titratable iodine
- For hospital or professional use only
Citric acid, Alkyl Polyglucoside, Nonylphenol ethoxylate, Sodium hydroxide, Purified water
|Labeler - Dukal Corporation (791014871)|
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