Label: IODINE PREP PAD ANTISEPTIC- povidone-iodine solution
- NDC Code(s): 72459-283-00
- Packager: Yiwu Ori-Power Medtech Co.,Ltd.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 18, 2024
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INGREDIENTS AND APPEARANCE
IODINE PREP PAD ANTISEPTIC
povidone-iodine solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72459-283 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 100 mg in 1 g Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) .BETA.-D-GLUCOPYRANOSE (UNII: J4R00M814D) HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D) NONOXYNOL-10 (UNII: K7O76887AP) GLYCERIN (UNII: PDC6A3C0OX) SODIUM HYDROXIDE (UNII: 55X04QC32I) POTASSIUM IODIDE (UNII: 1C4QK22F9J) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72459-283-00 0.55 g in 1 POUCH; Type 0: Not a Combination Product 02/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 02/01/2024 Labeler - Yiwu Ori-Power Medtech Co.,Ltd. (560451976)