BM POTASSIUM IODIDE (KALI IOD) 6X (bm potassium iodide- kali iod tablet

BM Potassium iodide (Kali Iod) 6X by

Drug Labeling and Warnings

BM Potassium iodide (Kali Iod) 6X by is a Homeopathic medication manufactured, distributed, or labeled by BM Private Limited. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

Directions:
Adult: Four tablets three times a day.
Ages below 12: half of the same or as prescribed by a homeopathic physician.

INACTIVE INGREDIENT

Inactive ingredients: Lactose; MAGNESIUM STEARATE

ACTIVE INGREDIENT

Potassium Iodide

INDICATIONS & USAGE

Uses
See the leaflet enclosed for detail.

PURPOSE

Uses
See the leaflet enclosed for detail.

CONTRAINDICATIONS

Contra-indications:
Traditional biochemic remedy do not interact with other remedies, herbs, or other supplements.

WARNINGS

Warnings and Storage:
Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.

KEEP OUT OF REACH OF CHILDREN

Warnings and Storage:
Ask a professional before use if pregnant or breastfeeding or if you have severe symptoms. Keep away from children. If you have a reaction to this product that is not positive, discontinue use. Store in a cool and dry place.

PRINCIPAL DISPLAY PANEL

Entire package

INGREDIENTS AND APPEARANCE

BM POTASSIUM IODIDE (KALI IOD) 6X 
bm potassium iodide (kali iod) tablet

Product 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)