POTASSIUM IODIDE- potassium iodide tablet tablet

Potassium Iodide by

Drug Labeling and Warnings

Potassium Iodide by is a Homeopathic medication manufactured, distributed, or labeled by Nature's Fusions, Llc, NATURE'S FUSIONS, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

FDA and CDC Recommended Dosage

150+lbs / Adult: 130mg (2 Tablets)
Children 3+ up to 150lbs: 65mg (1 Tablet)

WARNINGS AND PRECAUTIONS

Consult physician if pregnant/nursing, taking medication, or have a thyroid or medical condition. Keep out of reach of children. Store in
a cool, dry place.

Caution:

Consult physician if pregnant/nursing, taking medication, or have a thyroid or medical condition. Keep out of reach of children. Store in
a cool, dry place.

Inactive Ingredients

Microcrystalline Cellulose, Magnesium Stearate, Silicon Dioxide

Suggested Use:

Take as directed by physician or emergency personnel for short-term, emergency use only. Take daily dosage as recommended for no longer than 2 weeks.

Caution:

Keep out of reach of children.

Suggested Use:

For short-term, emergency use only.

Active Ingredients

Potassium Iodide

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

POTASSIUM IODIDE 
potassium iodide tablet tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73769-300
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)
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: O7TSZ97GEP)
MAGNESIUM STEARATE (UNII: 70097M6I30)

Product Characteristics
Color	white	Score	no score
Shape	ROUND	Size	8mm
Flavor		Imprint Code	none
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73769-300-40	140 in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2023
2	NDC: 73769-300-60	60 in 1 BOTTLE; Type 0: Not a Combination Product	04/01/2023
3	NDC: 73769-300-14	14 in 1 BOTTLE, GLASS; 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(73769-300)