Label: BM POTASSIUM IODIDE (KALI IOD) 6X (bm potassium iodide- kali iod tablet
- NDC Code(s): 85816-1033-1
- Packager: BM Private Limited
- 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 2, 2025
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- DOSAGE & ADMINISTRATION
- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
BM POTASSIUM IODIDE (KALI IOD) 6X
bm potassium iodide (kali iod) tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:85816-1033 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength POTASSIUM IODIDE (UNII: 1C4QK22F9J) (IODIDE ION - UNII:09G4I6V86Q) IODIDE ION 6 [hp_X] in 60 mg Inactive Ingredients Ingredient Name Strength LACTOSE (UNII: J2B2A4N98G) 58.75 mg in 60 mg MAGNESIUM STEARATE (UNII: 70097M6I30) 1.2 mg in 60 mg Product Characteristics Color white (WHITE DISSOLVABLE TABLETS) Score no score Shape ROUND (DISSOLVABLE TABLETS) Size 90mm Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:85816-1033-1 30000 mg in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 06/01/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/01/2025 Labeler - BM Private Limited (645599762) Establishment Name Address ID/FEI Business Operations BM Private Limited 645599762 manufacture(85816-1033) , label(85816-1033) , pack(85816-1033)

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