FDA.reportPublic FDA data

COLOCYNTHIS

Product NDC
60512-1014
11-digit product format
605121014
Labeler code
60512
Product ID
60512-1014_bb7ae816-f833-4c62-88a5-86b39b349299
Type
HUMAN OTC DRUG
Nonproprietary name
COLOCYNTHIS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CITRULLUS COLOCYNTHIS FRUIT PULP
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
60512-1014-12025-12-28C16284748780-19d75b9d0-b017-f424-e053-dadaa90a57ced87168ed-0f77-4a26-9b5b-4b54cc58d236
60512-1014-12020-01-31C16284748780-19d75b9d0-b017-f424-e053-dadaa90a57ced87168ed-0f77-4a26-9b5b-4b54cc58d236

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CITRULLUS COLOCYNTHIS FRUIT PULPACTIVE INGREDIENT23H32AOH17COLOCYNTHIS PELLET [HOMEOLAB USA INC.]1
CITRULLUS COLOCYNTHIS FRUIT PULPACTIVE MOIETY23H32AOH17COLOCYNTHIS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCOLOCYNTHIS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554COLOCYNTHIS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1014COLOCYNTHIS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131029_d87168ed-0f77-4a26-9b5b-4b54cc58d236.zip