FDA.reportPublic FDA data

ALUMEN

Product NDC
60512-6162
11-digit product format
605126162
Labeler code
60512
Product ID
60512-6162_84732b57-f1c1-40aa-81ec-904a5f940296
Type
HUMAN OTC DRUG
Nonproprietary name
ALUMEN
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ALUM, POTASSIUM
Active strength
3 [hp_X]/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-6162-12025-12-28C16284748780-19d75b9d0-db34-f424-e053-dadaa90a57ce9f5938ff-370f-4c0a-8151-b90349020104
60512-6162-12020-01-31C16284748780-19d75b9d0-db34-f424-e053-dadaa90a57ce9f5938ff-370f-4c0a-8151-b90349020104

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALUM, POTASSIUMACTIVE INGREDIENT1L24V9R23SALUMEN PELLET [HOMEOLAB USA INC.]1
ALUMINUM HYDROXIDEACTIVE MOIETY5QB0T2IUN0ALUMEN PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GALUMEN PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ALUMEN PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6162ALUMEN PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_9f5938ff-370f-4c0a-8151-b90349020104.zip