Label: QUALITY CHOICE POVIDONE IODINE- povidone iodine 10% liquid
- NDC Code(s): 63868-230-08
- Packager: Chain Drug Market Association
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 20, 2023
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- SPL UNCLASSIFIED SECTION
- Active Ingredient
- Purpose
- Use
- Warnings
- Ask a doctor before use if you have
- Stop use and consult a doctor if
- When using this product do not
- Keep out of reach of children.
- Directions
- Inactive Ingredients
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INGREDIENTS AND APPEARANCE
QUALITY CHOICE POVIDONE IODINE
povidone iodine 10% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-230 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 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERIN (UNII: PDC6A3C0OX) NONOXYNOL-9 (UNII: 48Q180SH9T) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-230-08 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/12/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 01/01/2008 Labeler - Chain Drug Market Association (011920774) Registrant - Pharma Nobis, LLC (118564114) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 manufacture(63868-230) , analysis(63868-230) , pack(63868-230) , label(63868-230)