FDA.reportPublic FDA data

NUX VOMICA

Product NDC
60512-1035
11-digit product format
605121035
Labeler code
60512
Product ID
60512-1035_bf3e089d-49f7-40de-9784-fd934554678d
Type
HUMAN OTC DRUG
Nonproprietary name
NUX VOMICA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
STRYCHNOS NUX-VOMICA SEED
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
60512-1035-12025-12-26C16284748780-19d75b9d0-3130-f424-e053-dadaa90a57ce17485071-4cf9-4013-9443-9669e9e6d1c7
60512-1035-12020-01-31C16284748780-19d75b9d0-3130-f424-e053-dadaa90a57ce17485071-4cf9-4013-9443-9669e9e6d1c7

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH13919NUX VOMICA PELLET [HOMEOLAB USA INC]1
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH13919NUX VOMICA PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GNUX VOMICA PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554NUX VOMICA PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1035NUX VOMICA PELLET [HOMEOLAB USA INC]1Legacy NDC20111207_17485071-4cf9-4013-9443-9669e9e6d1c7.zip