Povidone-iodine prep sterile sponge

Drug facts

Active ingredient

Povidone-Iodine USP 10%




For preparation prior to surgery Helps to reduce bacteria that can potentially cause skin infection.


For external use only.

Do not apply to persons allergic to iodine

Do not use

in the eyes

Ask a doctor before use if injuries are

deep wounds puncture wounds serious burns

Stop use and ask a doctor if

irritation and redness develop condition persists for more than 72 hours infection occurs

Avoid pooling beneath the patient.

Prolonged exposure to wet solution may cause skin irritation.

Keep out of reach of children.

If swallowed or gets in eyes, get medical help or contact a Poison Control Center right away.


Clean the area. Apply product to the operative site prior to surgery using sponge sticks to prep desired area.

Other information

1% titratable iodine latex free for hospital or professional use only

Inactive ingredients

Citric Acid, Alkyl Glucoside, Hydroxyethyl Cellulose, Nonoxynol-10, Glycerin, Sodium Hydroxide, Potassium Iodide, Purified Water

Ingredients and appearance - Product information

Povidone-iodine prep sterile sponge- Povidone-iodine

Product information

Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC: 63517-658
Route of Administration Topical

Active Ingredient/Active Moiety

Ingredient Name Strength
Povidone-iodine ( UNII: 85H0HZU99M)( Iodine - UNII: 9679TC07X4 ) 100 mgin 1 g

Inactive Ingredients

Ingredient Name Code
Citric acid monohydrate ( UNII: 2968PHW8QP)
Nonoxynol-10 ( UNII: K7O76887AP)
Glycerin ( UNII: PDC6A3C0OX)
Sodium hydroxide ( UNII: 55X04QC32I)
Potassium iodide ( UNII: 1C4QK22F9J)
Water ( UNII: 059QF0KO0R)

Product Characteristics


# Item Code Package Description Marketing Start Date
1 NDC: 63517-658-11 80g in 1 POUCH 2015/04/30

Marketing Information

Marketing Category Application Number or Monograph Citation Territorial Authority Marketing Start Date
OTC monograph not final part333E USA 2015/04/30

Labeler - Cardinal Health( 097537435)

Product label