Alumen

Product NDC
0220-0201
11-digit product format
002200201
Labeler code
0220
Product ID
0220-0201_15ecb7b6-bb34-adbe-e063-6294a90a57fd
Type
HUMAN OTC DRUG
Nonproprietary name
POTASSIUM ALUM
Dosage form
PELLET
Route
ORAL
Labeler
Boiron
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1983-03-03
Substance
POTASSIUM ALUM
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
Alumen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
POTASSIUM ALUM30 [hp_C]/30[hp_C]

Harmonized Identifiers#

Field, Values table
FieldValues
Unii1L24V9R23S

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0220-0201-412023-05-16C16284748780-1f386c64a-3d17-0266-e053-dadaa90a7c1aAlumen 30C
0220-0201-412023-01-30C16284748780-1f386c64a-3d17-0266-e053-dadaa90a7c1aAlumen 30C

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0201-41Alumen30 [hp_C] in 1 TUBEPELLET305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0220-0201ALUMEN (POTASSIUM ALUM) PELLET [BOIRON]5Current NDC, Legacy NDC, 1 package rows20240415_6922917a-8cb6-8557-e053-2991aa0a20fb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0220-0201-410022002014130 [hp_C] in 1 TUBE (0220-0201-41) 1983-03-030000-00-00NoNoCurrent