FDA.reportPublic FDA data

CYCLAMEN EUROPAEUM

Product NDC
60512-6634
11-digit product format
605126634
Labeler code
60512
Product ID
60512-6634_777fd8ce-4c4c-4cba-a31b-2b0b2131b830
Type
HUMAN OTC DRUG
Nonproprietary name
CYCLAMEN EUROPAEUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
CYCLAMEN PURPURASCENS TUBER
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
60512-6634-12025-12-26C16284748780-19d75b9cf-da2d-f424-e053-dadaa90a57ce9c91edd4-cd5f-4170-a492-cd81f0ecfaa2
60512-6634-12020-01-31C16284748780-19d75b9cf-da2d-f424-e053-dadaa90a57ce9c91edd4-cd5f-4170-a492-cd81f0ecfaa2

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CYCLAMEN PURPURASCENS TUBERACTIVE INGREDIENTG728143D8QCYCLAMEN EUROPAEUM PELLET [HOMEOLAB USA INC.]1
CYCLAMEN PURPURASCENS TUBERACTIVE MOIETYG728143D8QCYCLAMEN EUROPAEUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCYCLAMEN EUROPAEUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554CYCLAMEN EUROPAEUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6634CYCLAMEN EUROPAEUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_9c91edd4-cd5f-4170-a492-cd81f0ecfaa2.zip