FDA.reportPublic FDA data

ALUMINIUM MURIATICUM

Product NDC
60512-6163
11-digit product format
605126163
Labeler code
60512
Product ID
60512-6163_13ae0d37-c5f1-4fa7-a1c9-5387e82c38f4
Type
HUMAN OTC DRUG
Nonproprietary name
ALUMINIUM MURIATICUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ALUMINUM CHLORIDE
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
60512-6163-12025-12-28C16284748780-19d75b9d0-840a-f424-e053-dadaa90a57ce2bf44e9e-46a2-4edb-a787-1ae855d216ec
60512-6163-12020-01-31C16284748780-19d75b9d0-840a-f424-e053-dadaa90a57ce2bf44e9e-46a2-4edb-a787-1ae855d216ec

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ALUMINUM CHLORIDEACTIVE INGREDIENT3CYT62D3GAALUMINIUM MURIATICUM PELLET [HOMEOLAB USA INC.]1
ALUMINUM CATIONACTIVE MOIETY3XHB1D032BALUMINIUM MURIATICUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GALUMINIUM MURIATICUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ALUMINIUM MURIATICUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6163ALUMINIUM MURIATICUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131028_2bf44e9e-46a2-4edb-a787-1ae855d216ec.zip