Label: LUGOLS STRONG IODINE- iodine and potassium iodide solution
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Contains inactivated NDC Code(s)
NDC Code(s): 59365-6064-0, 59365-6064-1 - Packager: CooperSurgical, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated May 25, 2016
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- CONTENTS
- DESCRIPTION
- HOW SUPPLIED
- INDICATIONS AND USAGE
- ADMINISTRATION
- WARNINGS
- CONTRAINDICATIONS
- CAUTION
- STORAGE
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DISPOSAL
Opened containers with unused portions of product and applicator swabs containing residual product should be placed in a suitable, dry container for disposal following local hazardous waste practices. Waste containing LUGOL’S should not be subjected to any thermal process whether intended for destruction or recycling purposes.
- PRINCIPAL DISPLAY PANEL
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LUGOLS STRONG IODINE
iodine and potassium iodide solutionProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:59365-6064 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 0.05 g in 1 mL POTASSIUM IODIDE (UNII: 1C4QK22F9J) (IODIDE ION - UNII:09G4I6V86Q) POTASSIUM IODIDE 0.100 g in 1 mL Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59365-6064-1 12 in 1 CARTON 10/01/1992 1 NDC:59365-6064-0 8 mL in 1 VIAL, SINGLE-USE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 10/01/1992 Labeler - CooperSurgical, Inc. (801895244)