FDA.reportPublic FDA data

CALCAREA SULPHURICA

Product NDC
60512-1010
11-digit product format
605121010
Labeler code
60512
Product ID
60512-1010_2bf2a090-9000-46d3-b823-8a6fc69f6879
Type
HUMAN OTC DRUG
Nonproprietary name
CALCAREA SULPHURICA
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 SULFATE
Active strength
6 [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
60512-1010-12025-12-29C16284748780-19d75b9cf-d475-f424-e053-dadaa90a57ce285ed194-fc0f-4f1c-bd76-b9a87ff8227c
60512-1010-12020-01-31C16284748780-19d75b9cf-d475-f424-e053-dadaa90a57ce285ed194-fc0f-4f1c-bd76-b9a87ff8227c

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CALCIUM SULFATEACTIVE INGREDIENTWAT0DDB505CALCAREA SULPHURICA PELLET [HOMEOLAB USA INC.]1
CALCIUM CATIONACTIVE MOIETY2M83C4R6ZBCALCAREA SULPHURICA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCALCAREA SULPHURICA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554CALCAREA SULPHURICA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1010CALCAREA SULPHURICA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131029_285ed194-fc0f-4f1c-bd76-b9a87ff8227c.zip