FDA.reportPublic FDA data

AURUM METALLICUM

Product NDC
60512-8001
11-digit product format
605128001
Labeler code
60512
Product ID
60512-8001_10adc95b-429b-4b77-9afd-ee7435778e1d
Type
HUMAN OTC DRUG
Nonproprietary name
AURUM METALLICUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
GOLD
Active strength
8 [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
60512-8001-12025-12-28C16284748780-19d75b9d0-5dca-f424-e053-dadaa90a57ceb035b0e0-fae6-4581-8609-0981983606e2
60512-8001-12020-01-31C16284748780-19d75b9d0-5dca-f424-e053-dadaa90a57ceb035b0e0-fae6-4581-8609-0981983606e2

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GOLDACTIVE INGREDIENT79Y1949PYOAURUM METALLICUM PELLET [HOMEOLAB USA INC.]1
GOLDACTIVE MOIETY79Y1949PYOAURUM METALLICUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAURUM METALLICUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554AURUM METALLICUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-8001AURUM METALLICUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_b035b0e0-fae6-4581-8609-0981983606e2.zip