Kali iodatum

Product NDC
0220-2802
11-digit product format
002202802
Labeler code
0220
Product ID
0220-2802_f529227e-4142-fc0b-e053-2a95a90a8c50
Type
HUMAN OTC DRUG
Nonproprietary name
POTASSIUM IODIDE
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
POTASSIUM IODIDE
Active strength
30 [hp_C]/30[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Kali iodatum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
POTASSIUM IODIDE30 [hp_C]/30[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1C4QK22F9J

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-2802-412023-02-20C16284748780-1f386c64a-0a08-0266-e053-dadaa90a7c1aKali iodatum 30C
0220-2802-412023-01-30C16284748780-1f386c64a-0a08-0266-e053-dadaa90a7c1aKali iodatum 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-2802-41Kali iodatum30 [hp_C] in 1 TUBEPELLET302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-2802KALI IODATUM (POTASSIUM IODIDE ) PELLET [BOIRON]2Current NDC, Legacy NDC, 1 package rows20230222_8607b598-935f-1581-e053-2991aa0afb11.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-2802-410022028024130 [hp_C] in 1 TUBE (0220-2802-41) 1983-03-030000-00-00NoNoCurrent