FDA.reportPublic FDA data

HEPAR SULPHURIS CALCAREUM

Product NDC
60512-1022
11-digit product format
605121022
Labeler code
60512
Product ID
60512-1022_a2505ba9-79d5-45ca-8f4a-ff4d952f4924
Type
HUMAN OTC DRUG
Nonproprietary name
HEPAR SULPHURIS CALCAREUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CALCIUM SULFIDE
Active strength
1 [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
60512-1022-12025-12-28C16284748780-19d75b9d1-082b-f424-e053-dadaa90a57cecf412075-bc67-4f79-bac2-dc596eb0f838
60512-1022-12020-01-31C16284748780-19d75b9d1-082b-f424-e053-dadaa90a57cecf412075-bc67-4f79-bac2-dc596eb0f838

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CALCIUM SULFIDEACTIVE INGREDIENT1MBW07J51QHEPAR SULPHURIS CALCAREUM PELLET [HOMEOLAB USA INC]1
CALCIUM CATIONACTIVE MOIETY2M83C4R6ZBHEPAR SULPHURIS CALCAREUM PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GHEPAR SULPHURIS CALCAREUM PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554HEPAR SULPHURIS CALCAREUM PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1022HEPAR SULPHURIS CALCAREUM PELLET [HOMEOLAB USA INC]1Legacy NDC20111205_cf412075-bc67-4f79-bac2-dc596eb0f838.zip