NATRUM SULPHURICUM

Product NDC
60512-8032
11-digit product format
605128032
Labeler code
60512
Product ID
60512-8032_532924b7-d092-4bef-a044-ef748b59d0d3
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
12 [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
60512-8032NATRUM SULPHURICUM TABLET, CHEWABLE [HOMEOLAB USA INC]1Legacy NDC20140325_a38db29a-04c6-49be-bd85-8e9cb66359fc.zip