Label: RITE AID POVIDONE IODINE- povidone iodine 10% liquid
- NDC Code(s): 11822-3775-7
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 15, 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
- Other information
- Inactive Ingredients
- Label
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INGREDIENTS AND APPEARANCE
RITE AID POVIDONE IODINE
povidone iodine 10% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-3775 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 GLYCERIN (UNII: PDC6A3C0OX) NONOXYNOL-9 (UNII: 48Q180SH9T) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-3775-7 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/14/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 01/01/2008 Labeler - Rite Aid Corporation (014578892) Registrant - Pharma Nobis, LLC (118564114) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 manufacture(11822-3775) , analysis(11822-3775) , pack(11822-3775) , label(11822-3775)