Label: POVIDONE IODINE solution
- NDC Code(s): 34645-4009-6
- Packager: Jianerkang Medical Co., Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 23, 2023
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- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- Other information
- INACTIVE INGREDIENT
- Package label
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INGREDIENTS AND APPEARANCE
POVIDONE IODINE
povidone iodine solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:34645-4009 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 7.5 mg in 1 mL Inactive Ingredients Ingredient Name Strength CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) NONOXYNOL-10 (UNII: K7O76887AP) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:34645-4009-6 109 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 01/01/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M005 01/01/2010 Labeler - Jianerkang Medical Co., Ltd (530968767) Establishment Name Address ID/FEI Business Operations Jianerkang Medical Co., Ltd 530968767 manufacture(34645-4009)