KALI SULPHURICUM

Product NDC
60512-8023
11-digit product format
605128023
Labeler code
60512
Product ID
60512-8023_e07c4129-87d7-4ffb-9259-561568930826
Type
HUMAN OTC DRUG
Nonproprietary name
KALI SULPHURICUM
Dosage form
TABLET, CHEWABLE
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2014-03-19
Marketing end
0000-00-00
Substance
POTASSIUM 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
POTASSIUM SULFATEACTIVE INGREDIENT1K573LC5TVKALI SULPHURICUM TABLET, CHEWABLE [HOMEOLAB USA INC]1
SULFATE IONACTIVE MOIETY7IS9N8KPMGKALI SULPHURICUM TABLET, CHEWABLE [HOMEOLAB USA INC]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XKALI SULPHURICUM TABLET, CHEWABLE [HOMEOLAB USA INC]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30KALI SULPHURICUM TABLET, CHEWABLE [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-8023KALI SULPHURICUM TABLET, CHEWABLE [HOMEOLAB USA INC]1Legacy NDC20140320_a8b44efc-c7dc-4b8c-843b-70e13179f4ce.zip