Label: POTASSIUM IODIDE capsule
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Contains inactivated NDC Code(s)
NDC Code(s): 73769-301-40, 73769-301-60 - Packager: NATURE'S FUSIONS, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated December 7, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- FDA and CDC Recommended Dosage
- WARNINGS AND PRECAUTIONS
- Caution:
- Inactive Ingredients
- Suggested Use:
- Caution:
- Suggested Use:
- Active Ingredients
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
POTASSIUM IODIDE
potassium iodide capsuleProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73769-301 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM IODIDE (UNII: 1C4QK22F9J) (IODIDE ION - UNII:09G4I6V86Q) POTASSIUM IODIDE 65 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U) MAGNESIUM STEARATE (UNII: 70097M6I30) CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP) HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH) Product Characteristics Color white Score no score Shape CAPSULE (Size 1) Size 7mm Flavor Imprint Code none Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73769-301-40 140 in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2023 2 NDC:73769-301-60 60 in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 04/01/2023 Labeler - NATURE'S FUSIONS, LLC (051472644) Establishment Name Address ID/FEI Business Operations NATURE'S FUSIONS, LLC 051472644 manufacture(73769-301)