Label: PVP-I PREP PADS FOIL-FOIL- povidone-iodine swab
- NDC Code(s): 65517-0034-1, 65517-0034-2
- Packager: Dukal LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 28, 2024
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- Active Ingredient:
- Purpose:
- Use:
- Warnings:
- DO NOT USE
- Directions:
- Other Information:
- Inactive Ingredients:
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Principal Display Panel - PVP-I Prep Pads Foil Pouch Label
Dukal
Povidone-Iodine Prep PadSterile
Antiseptic
For Professional and Hospital Use
Not made with natura rubber latex
Sterile unless package is damaged or opened.
Manufactured For: Dukal, LLC
1(800)243-0741 / Ronkonkoma, NY 11779 / dukal.com
Made in China
Dukal is a trademark registered in the
US Patent & Trademark Office by Dukal, LLC
1 Per Pouch - 2 - NDC 6551-0034-1 - REF 882
-
Principal Display Panel - PVP-I Prep Pads Paper Pouch Label
Dukal
Povidone-Iodine Prep PadSterile
Antiseptic
For Professional and Hospital Use
Not made with natura rubber latex
Sterile unless package is damaged or opened.
Manufactured For: Dukal, LLC
1(800)243-0741 / Ronkonkoma, NY 11779 / dukal.com
Made in China
Dukal is a trademark registered in the
US Patent & Trademark Office by Dukal, LLC Rev1
1 Per Pouch - 2 - NDC 6551-0034-2 - REF 889
-
INGREDIENTS AND APPEARANCE
PVP-I PREP PADS FOIL-FOIL
povidone-iodine swabProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65517-0034 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 1 g in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16) NONOXYNOL-10 (UNII: K7O76887AP) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA) POTASSIUM IODIDE (UNII: 1C4QK22F9J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65517-0034-1 8000 in 1 CASE 01/31/2018 1 0.5 mL in 1 POUCH; Type 0: Not a Combination Product 2 NDC:65517-0034-2 4000 in 1 CASE 01/31/2018 2 0.5 mL in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 01/31/2018 Labeler - Dukal LLC (791014871)