FDA.reportPublic FDA data

DULCAMARA

Product NDC
60512-1016
11-digit product format
605121016
Labeler code
60512
Product ID
60512-1016_5cd9cd5e-f893-446d-abec-db99415bf4bf
Type
HUMAN OTC DRUG
Nonproprietary name
DULCAMARA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-11-18
Marketing end
0000-00-00
Substance
SOLANUM DULCAMARA TOP
Active strength
2 [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
60512-1016-12025-12-31C16284748780-19d75b9d0-b5cf-f424-e053-dadaa90a57cee34e6cbd-cd68-4fea-80de-b379d76d8850
60512-1016-12020-01-31C16284748780-19d75b9d0-b5cf-f424-e053-dadaa90a57cee34e6cbd-cd68-4fea-80de-b379d76d8850

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SOLANUM DULCAMARA TOPACTIVE INGREDIENTKPS1B1162NDULCAMARA PELLET [HOMEOLAB USA INC.]1
SOLANUM DULCAMARA TOPACTIVE MOIETYKPS1B1162NDULCAMARA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GDULCAMARA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554DULCAMARA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1016DULCAMARA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_e34e6cbd-cd68-4fea-80de-b379d76d8850.zip