FDA.reportPublic FDA data

AETHUSA CYNAPIUM

Product NDC
60512-6450
11-digit product format
605126450
Labeler code
60512
Product ID
60512-6450_91caf524-af9e-417d-9050-84826200bc46
Type
HUMAN OTC DRUG
Nonproprietary name
AETHUSA CYNAPIUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
AETHUSA CYNAPIUM
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
60512-6450-12025-12-28C16284748780-19d75b9d0-004c-f424-e053-dadaa90a57ce997087cf-cda6-45b2-85dd-991a84971a4e
60512-6450-12020-01-31C16284748780-19d75b9d0-004c-f424-e053-dadaa90a57ce997087cf-cda6-45b2-85dd-991a84971a4e

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AETHUSA CYNAPIUMACTIVE INGREDIENTM6936L953CAETHUSA CYNAPIUM PELLET [HOMEOLAB USA INC.]1
AETHUSA CYNAPIUMACTIVE MOIETYM6936L953CAETHUSA CYNAPIUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAETHUSA CYNAPIUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554AETHUSA CYNAPIUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6450AETHUSA CYNAPIUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_997087cf-cda6-45b2-85dd-991a84971a4e.zip