FDA.reportPublic FDA data

RUTA GRAVEOLENS

Product NDC
60512-1041
11-digit product format
605121041
Labeler code
60512
Product ID
60512-1041_60bb4223-c894-4dbd-8b16-49b2424893b7
Type
HUMAN OTC DRUG
Nonproprietary name
RUTA GRAVEOLENS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
RUTA GRAVEOLENS FLOWERING TOP
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
60512-1041-12025-12-29C16284748780-19d75b9cf-d48d-f424-e053-dadaa90a57ce6839b8fd-58bf-4c5c-bf05-13d6ff3f9468
60512-1041-12020-01-31C16284748780-19d75b9cf-d48d-f424-e053-dadaa90a57ce6839b8fd-58bf-4c5c-bf05-13d6ff3f9468

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
RUTA GRAVEOLENS FLOWERING TOPACTIVE INGREDIENTN94C2U587SRUTA GRAVEOLENS PELLET [HOMEOLAB USA INC.]1
RUTA GRAVEOLENS FLOWERING TOPACTIVE MOIETYN94C2U587SRUTA GRAVEOLENS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GRUTA GRAVEOLENS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554RUTA GRAVEOLENS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1041RUTA GRAVEOLENS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131029_6839b8fd-58bf-4c5c-bf05-13d6ff3f9468.zip