NATRUM SULPHURICUM

Product NDC
60512-8031
11-digit product format
605128031
Labeler code
60512
Product ID
60512-8031_73e128ba-b414-4d87-89f6-b5ee06032d6a
Type
HUMAN OTC DRUG
Nonproprietary name
NATRUM SULPHURICUM
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2014-03-25
Marketing end
0000-00-00
Substance
SODIUM 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#

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SODIUM SULFATEACTIVE INGREDIENT0YPR65R21JNATRUM SULPHURICUM TABLET, CHEWABLE [HOMEOLAB USA INC]1
SODIUM SULFATE ANHYDROUSACTIVE MOIETY36KCS0R750NATRUM SULPHURICUM TABLET, CHEWABLE [HOMEOLAB USA INC]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XNATRUM SULPHURICUM TABLET, CHEWABLE [HOMEOLAB USA INC]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30NATRUM SULPHURICUM TABLET, CHEWABLE [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-8031NATRUM SULPHURICUM TABLET, CHEWABLE [HOMEOLAB USA INC]1Legacy NDC20140325_b82c9223-7aaa-4c81-970e-c7d3e4358811.zip