Label: LUGOLS SOLUTION- lugols liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 10481-0111-8 - Packager: Gordon Laboratories
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated February 1, 2010
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- DESCRIPTION
- HOW SUPPLIED
- SPL UNCLASSIFIED SECTION
- WARNINGS AND PRECAUTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LUGOLS SOLUTION
lugols liquidProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:10481-0111 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 0.4 g in 1 g Inactive Ingredients Ingredient Name Strength POTASSIUM IODIDE (UNII: 1C4QK22F9J) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10481-0111-8 8 g in 1 BOTTLE, GLASS Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 02/01/2010 Labeler - Gordon Laboratories (002333847) Registrant - Gordon Laboratories (002333847) Establishment Name Address ID/FEI Business Operations Gordon Laboratories 002333847 manufacture