FDA.reportPublic FDA data

MERCURIUS VIVUS

Product NDC
60512-1031
11-digit product format
605121031
Labeler code
60512
Product ID
60512-1031_59e5feea-a351-48ca-8ba6-be8562eb722f
Type
HUMAN OTC DRUG
Nonproprietary name
MERCURIUS VIVUS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
MERCURY
Active strength
6 [hp_X]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-1031-12025-12-29C16284748780-19d75b9d0-3f1f-f424-e053-dadaa90a57cef7809f51-8080-4fe0-99ad-a912d713497d
60512-1031-12020-01-31C16284748780-19d75b9d0-3f1f-f424-e053-dadaa90a57cef7809f51-8080-4fe0-99ad-a912d713497d

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MERCURYACTIVE INGREDIENTFXS1BY2PGLMERCURIUS VIVUS PELLET [HOMEOLAB USA INC]1
MERCURYACTIVE MOIETYFXS1BY2PGLMERCURIUS VIVUS PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GMERCURIUS VIVUS PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554MERCURIUS VIVUS PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1031MERCURIUS VIVUS PELLET [HOMEOLAB USA INC]1Legacy NDC20111207_f7809f51-8080-4fe0-99ad-a912d713497d.zip