FDA.reportPublic FDA data

NATRUM SULPHURICUM

Product NDC
60512-1034
11-digit product format
605121034
Labeler code
60512
Product ID
60512-1034_70be8665-a7ba-498d-b7a8-355eac13109a
Type
HUMAN OTC DRUG
Nonproprietary name
NATRUM SULPHURICUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
SODIUM SULFATE
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
60512-1034-12025-12-29C16284748780-19d75b9d0-2b03-f424-e053-dadaa90a57ce981e03d7-b604-4fbb-bc29-b4520e90fd58
60512-1034-12020-01-31C16284748780-19d75b9d0-2b03-f424-e053-dadaa90a57ce981e03d7-b604-4fbb-bc29-b4520e90fd58

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM SULFATEACTIVE INGREDIENT0YPR65R21JNATRUM SULPHURICUM PELLET [HOMEOLAB USA INC.]1
SODIUM SULFATE ANHYDROUSACTIVE MOIETY36KCS0R750NATRUM SULPHURICUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GNATRUM SULPHURICUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554NATRUM SULPHURICUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1034NATRUM SULPHURICUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131029_981e03d7-b604-4fbb-bc29-b4520e90fd58.zip