Label: LUGOLS SOLUTION - lugols liquid
- 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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Updated February 1, 2010
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Strong Iodine Solution USP a topical anti-infective agent.Close
- HOW SUPPLIED
Applied with a q-tip.
- SPL UNCLASSIFIED SECTION
May be stored at room temperature.Close
- WARNINGS AND PRECAUTIONS
Single use only. Do not reuse. Discard after one use. Do not use if seal is broken. Restricted to use by or on the order of a licensed Physician. Keep cap tightly sealed and product from light.
- INGREDIENTS AND APPEARANCE
Product 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