Label: IODINE liquid
- NDC Code(s): 50804-088-10
- Packager: Perrigo Direct, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated November 18, 2022
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- Active Ingredient
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INGREDIENTS AND APPEARANCE
IODINE
iodine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50804-088 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 20 mg in 1 mL SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q) IODIDE ION 20.4 mg in 1 mL ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 470 mg in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50804-088-10 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/08/2008 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 11/08/2008 Labeler - Perrigo Direct, Inc. (076059836) Registrant - Vi-Jon, LLC (088520668) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 manufacture(50804-088)