Label: IODINE- iodine alcoholic solution
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Contains inactivated NDC Code(s)
NDC Code(s): 16638-166-38 - Packager: Borisovskiy Zavod Medicinskikh Preparatov JSC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
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Drug Label Information
Updated November 26, 2015
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INGREDIENTS AND APPEARANCE
IODINE
iodine alcoholic solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:16638-166 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE 0.5 g in 10 mL POTASSIUM IODIDE (UNII: 1C4QK22F9J) (IODIDE ION - UNII:09G4I6V86Q) IODIDE ION 0.2 g in 10 mL Inactive Ingredients Ingredient Name Strength ETHANOL, 2-(BIS(2-METHYLPROPYL)PHENOXY)- (UNII: AUK0O5KW1Y) 10 mL in 10 mL WATER (UNII: 059QF0KO0R) 10 mL in 10 mL Product Characteristics Color brown (Transparent red-brown liquid) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:16638-166-38 10 mL in 1 VIAL; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/20/1999 Labeler - Borisovskiy Zavod Medicinskikh Preparatov JSC (628149593) Establishment Name Address ID/FEI Business Operations Borisovskiy Zavod Medicinskikh Preparatov JSC 628149593 manufacture(16638-166)