Label: QUALITY CHOICE IODINE TINCTURE MILD- iodine and sodium iodide and alcohol liquid
- NDC Code(s): 63868-330-01
- Packager: Chain Drug Market Association
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 20, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Indications
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Warnings
For external use only.
Ask a doctor before use if you have
- deep or puncture wounds
- animal bites
- serious burns
- Flammable: Keep away from sparks heat and flame
Stop use and consult doctor if
- the condition persists or gets worse, or if using for longer than one week
- deep or puncture wounds
- Directions
- Other information
- Inactive ingredient
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
QUALITY CHOICE IODINE TINCTURE MILD
iodine and sodium iodide and alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-330 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:63868-330-01 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 12/12/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M003 01/01/1979 Labeler - Chain Drug Market Association (011920774) Registrant - Pharma Nobis, LLC (118564114) Establishment Name Address ID/FEI Business Operations Pharma Nobis, LLC 118564114 manufacture(63868-330) , analysis(63868-330) , pack(63868-330) , label(63868-330)