FDA.reportPublic FDA data

COLOCYNTHIS

Product NDC
60512-6615
11-digit product format
605126615
Labeler code
60512
Product ID
60512-6615_c3afa8e0-ccb7-43ea-9fa4-ac5071bcf382
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
60512-6615-12025-12-29C16284748780-19d75b9cf-d47b-f424-e053-dadaa90a57ce59f9b708-f499-4b83-9216-6783bad75c1f
60512-6615-12020-01-31C16284748780-19d75b9cf-d47b-f424-e053-dadaa90a57ce59f9b708-f499-4b83-9216-6783bad75c1f

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
60512-6615COLOCYNTHIS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131029_59f9b708-f499-4b83-9216-6783bad75c1f.zip