FDA.reportPublic FDA data

CHELIDONIUM MAJUS

Product NDC
60512-6585
11-digit product format
605126585
Labeler code
60512
Product ID
60512-6585_5f047a70-8592-422b-94f8-242231383f91
Type
HUMAN OTC DRUG
Nonproprietary name
CHELIDONIUM MAJUS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CHELIDONIUM MAJUS
Active strength
1 [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
60512-6585-12025-12-27C16284748780-19d75b9d0-e173-f424-e053-dadaa90a57ce47725769-4b5b-4e63-8162-2584bae337a0
60512-6585-12020-01-31C16284748780-19d75b9d0-e173-f424-e053-dadaa90a57ce47725769-4b5b-4e63-8162-2584bae337a0

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CHELIDONIUM MAJUSACTIVE INGREDIENT7E889U5RNNCHELIDONIUM MAJUS PELLET [HOMEOLAB USA INC.]1
CHELIDONIUM MAJUSACTIVE MOIETY7E889U5RNNCHELIDONIUM MAJUS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCHELIDONIUM MAJUS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554CHELIDONIUM MAJUS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6585CHELIDONIUM MAJUS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_47725769-4b5b-4e63-8162-2584bae337a0.zip