Label: FIRST AID ANTISEPTIC- povidone-iodine solution
- NDC Code(s): 11822-9050-1
- Packager: Rite Aid
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 18, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- uses
- Warnings
- Do not use
- Ask a doctor before use
- stop use and ask a doctor if
- Keep out of reach of children.
- Directions
- Other inforamation
- inactive ingredents
- Disclaimer
- Adverse Reactions
- principal display panel
-
INGREDIENTS AND APPEARANCE
FIRST AID ANTISEPTIC
povidone-iodine solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-9050 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 C12-13 PARETH-9 (UNII: 9BXD858P37) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) GLYCERIN (UNII: PDC6A3C0OX) SODIUM HYDROXIDE (UNII: 55X04QC32I) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-9050-1 237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/18/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 11/18/2024 Labeler - Rite Aid (014578892) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(11822-9050)