FDA.reportPublic FDA data

CAUSTICUM

Product NDC
60512-6228
11-digit product format
605126228
Labeler code
60512
Product ID
60512-6228_3f9ec2bf-dee2-4b39-b752-5254c3164e9b
Type
HUMAN OTC DRUG
Nonproprietary name
CAUSTICUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CAUSTICUM
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
60512-6228-12025-12-28C16284748780-19d75b9d0-5ddf-f424-e053-dadaa90a57ce57f6de2e-6712-4a59-af2a-2519d1742050
60512-6228-12020-01-31C16284748780-19d75b9d0-5ddf-f424-e053-dadaa90a57ce57f6de2e-6712-4a59-af2a-2519d1742050

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CAUSTICUMACTIVE INGREDIENTDD5FO1WKFUCAUSTICUM PELLET [HOMEOLAB USA INC.]1
CAUSTICUMACTIVE MOIETYDD5FO1WKFUCAUSTICUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCAUSTICUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554CAUSTICUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6228CAUSTICUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_57f6de2e-6712-4a59-af2a-2519d1742050.zip