Label: GNP IDOINDE TINCTURE 2% MILD- iodine and sodium iodide and alcohol liquid
- NDC Code(s): 24385-213-10
- Packager: Amerisource Bergen
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 14, 2023
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- Active Ingredients
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- Uses:
- Warnings:
- Ask a doctor before use if you have
- Stop use and ask a doctor if
- When using this product.
- Keep out of reach ofchildren
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INGREDIENTS AND APPEARANCE
GNP IDOINDE TINCTURE 2% MILD
iodine and sodium iodide and alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24385-213 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:24385-213-10 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/16/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 01/01/2008 Labeler - Amerisource Bergen (007914906) Registrant - Pharma Nobis, LLC (118564114) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 manufacture(24385-213) , analysis(24385-213) , pack(24385-213) , label(24385-213)