Label: POVIDONE-IODINE 10% SOLUTION- povidone iodine 10% liquid liquid
- NDC Code(s): 82429-202-16
- Packager: Gabar Health Sciences Corp.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 21, 2023
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- ACTIVE INGREDIENT
- Warnings
- Do Not Use
- Stop use and ask a doctor if
- KEEP OUT OF REACH OF CHILDREN
- Inactive Ingredients
- Purpose
- Use
- Use
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INGREDIENTS AND APPEARANCE
POVIDONE-IODINE 10% SOLUTION
povidone iodine 10% liquid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82429-202 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T) GLYCERIN (UNII: PDC6A3C0OX) POLYSORBATE 80 (UNII: 6OZP39ZG8H) WATER (UNII: 059QF0KO0R) SODIUM CITRATE (UNII: 1Q73Q2JULR) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82429-202-16 3780 mL in 1 PACKAGE; Type 0: Not a Combination Product 10/10/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 10/10/2022 Labeler - Gabar Health Sciences Corp. (118401847) Registrant - Gabar Health Sciences Corp. (118401847)