FDA.reportPublic FDA data

Potassium Iodide Tablet

Manufacturer
Nature's Fusions, Llc
Effective date
2023-12-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:24:59

Label at a glance#

ProductPotassium Iodide
Active ingredientPOTASSIUM IODIDE
Label structure9 sections

Label contents#

Full prescribing information#

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

14 Count KI Tablets14 Count KI Tablets60 Count Ki Tablets60 Count Ki Tablets140 Ct Ki Tablets140 Ct Ki Tablets

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73769-300-142025-01-30C16284748780-12cef2736-a338-d83d-e063-dadaa90ab31fPotassium Iodide Tablet
73769-300-402025-01-30C16284748780-12cef2736-a338-d83d-e063-dadaa90ab31fPotassium Iodide Tablet
73769-300-602025-01-30C16284748780-12cef2736-a338-d83d-e063-dadaa90ab31fPotassium Iodide Tablet

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73769-300-14Potassium Iodide14 in 1 BOTTLE, GLASSTABLET141
73769-300-40Potassium Iodide140 in 1 BOTTLETABLET1401
73769-300-60Potassium Iodide60 in 1 BOTTLETABLET601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73769-300POTASSIUM IODIDE (POTASSIUM IODIDE TABLET) TABLET [NATURE'S FUSIONS, LLC]13 package rows20231207_0bde56be-868f-d1cd-e063-6294a90abe45.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73769-30073769-300-40, 73769-300-60, 73769-300-14

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
SILICON DIOXIDEETJ7Z6XBU4IACT
CELLULOSE, MICROCRYSTALLINEOP1R32D61UIACT
CALCIUM PHOSPHATE, DIBASIC, DIHYDRATEO7TSZ97GEPIACT
POTASSIUM IODIDE1C4QK22F9JACTIB
MAGNESIUM STEARATE70097M6I30IACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0bde56be-8690-d1cd-e063-6294a90abe450bde56be-868f-d1cd-e063-6294a90abe452023-12-06WarningsExact identifier
spl id: 0bde56be-8690-d1cd-e063-6294a90abe45
spl set id: 0bde56be-868f-d1cd-e063-6294a90abe45

Reported adverse events (FAERS/openFDA)#

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