Potassium Iodide

Manufacturer: NATURE'S FUSIONS, LLC
Effective date: 2023-12-07
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:25:00

Label at a glance#

ProductPotassium Iodide

Active ingredientPOTASSIUM IODIDE

Label structure9 sections

Label contents#

Full prescribing information#

FDA and CDC Recommended Dosage

DOSAGE & ADMINISTRATION SECTION

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

WARNINGS AND PRECAUTIONS SECTION

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:

WARNINGS SECTION

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

INACTIVE INGREDIENT SECTION

Microcrystalline Cellulose, Magnesium Stearate, Silicon Dioxide

Suggested Use:

INDICATIONS & USAGE SECTION

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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Suggested Use:

OTC - PURPOSE SECTION

For short-term, emergency use only.

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Potassium Iodide

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

140 Ct Ki Capsules

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73769-301-40	2025-01-30	C162847	48780-1	2cef2736-918a-d83d-e063-dadaa90ab31f	Potassium Iodide
73769-301-60	2025-01-30	C162847	48780-1	2cef2736-918a-d83d-e063-dadaa90ab31f	Potassium Iodide

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73769-301-40	Potassium Iodide	140 in 1 BOTTLE	CAPSULE	140		1
73769-301-60	Potassium Iodide	60 in 1 BOTTLE	CAPSULE	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73769-301	POTASSIUM IODIDE CAPSULE [NATURE'S FUSIONS, LLC]	1	2 package rows	20231208_0bf3ceba-d76f-adc3-e063-6294a90a06b9.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

Potassium Iodide
SILICON DIOXIDE
CELLULOSE, MICROCRYSTALLINE
MAGNESIUM STEARATE
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE
IODIDE ION
HYDROXYPROPYL CELLULOSE, UNSPECIFIED

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73769-301	73769-301-40, 73769-301-60

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
CELLULOSE, MICROCRYSTALLINE	OP1R32D61U	IACT
MAGNESIUM STEARATE	70097M6I30	IACT
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATE	O7TSZ97GEP	IACT
POTASSIUM IODIDE	1C4QK22F9J	ACTIB
HYDROXYPROPYL CELLULOSE, UNSPECIFIED	9XZ8H6N6OH	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0bf3ceba-d770-adc3-e063-6294a90a06b9			0bf3ceba-d76f-adc3-e063-6294a90a06b9	2023-12-07	Warnings	Exact identifier spl id: 0bf3ceba-d770-adc3-e063-6294a90a06b9 spl set id: 0bf3ceba-d76f-adc3-e063-6294a90a06b9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.