Povidone Iodine Solution

Dosage Form: topical solution

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


Povidone-Iodine


In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.



Antiseptic skin preparation

Do not use if allergic to iodine

For external use only

Ask a doctor before use if injuries are

  • deep or punture wounds
  • serious burns
Stop use and ask a doctor if

  • redness, irritation, swelling or pain persists or increases
  • infection occurs
Do not use in eyes

Avoid pooling beneath patient

Keep out of reach of children

In case of accidental ingestion, seek professional assistance or consult a poison
control center immediately.

Apply locally as needed

citric acid, disodium phosphate,

nonoxynol-9, sodium hydroxide, water

Povidone Packet image.jpg

Antiseptic

POVIDONE-IODINE 
povidone-iodine solution
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:51688-5473
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Povidone-Iodine (Povidone-Iodine) Povidone-Iodine 9.8 g  in 100 g
Inactive Ingredients
Ingredient Name Strength
Citric Acid Monohydrate  
Sodium Phosphate, DIBASIC  
Sodium Hydroxide  
Nonoxynol-9  
Water  
Packaging
# Item Code Package Description
1 NDC:51688-5473-2 9.8 g in 1 PACKET
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph not final part333A 01/03/1984
Labeler - Smiths Medical ASD, INC (137835299)
Revised: 07/2010
 
Smiths Medical ASD, INC



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