FDA.reportPublic FDA data

GELSEMIUM SEMPERVIRENS

Product NDC
60512-1020
11-digit product format
605121020
Labeler code
60512
Product ID
60512-1020_b72e0200-e739-4552-9188-976bced2a0dc
Type
HUMAN OTC DRUG
Nonproprietary name
GELSEMIUM SEMPERVIRENS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
GELSEMIUM SEMPERVIRENS ROOT
Active strength
3 [hp_X]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-1020-12025-12-31C16284748780-19d75b9d0-97a8-f424-e053-dadaa90a57ce966e3d7c-df42-400a-960b-17d9dd3752ec
60512-1020-12020-01-31C16284748780-19d75b9d0-97a8-f424-e053-dadaa90a57ce966e3d7c-df42-400a-960b-17d9dd3752ec

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
GELSEMIUM SEMPERVIRENS ROOTACTIVE INGREDIENT639KR60Q1QGELSEMIUM SEMPERVIRENS PELLET [HOMEOLAB USA INC]1
GELSEMIUM SEMPERVIRENS ROOTACTIVE MOIETY639KR60Q1QGELSEMIUM SEMPERVIRENS PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GGELSEMIUM SEMPERVIRENS PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554GELSEMIUM SEMPERVIRENS PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1020GELSEMIUM SEMPERVIRENS PELLET [HOMEOLAB USA INC]1Legacy NDC20111205_966e3d7c-df42-400a-960b-17d9dd3752ec.zip