FDA.reportPublic FDA data

BELLIS PERENNIS

Product NDC
60512-6541
11-digit product format
605126541
Labeler code
60512
Product ID
60512-6541_d6d268f8-a9ed-429f-ac4c-26ca154f5e6a
Type
HUMAN OTC DRUG
Nonproprietary name
BELLIS PERENNIS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
BELLIS PERENNIS
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
60512-6541-12025-12-28C16284748780-19d75b9d0-5dc7-f424-e053-dadaa90a57ce48fa4cda-2a3f-4e15-b626-673100b4f923
60512-6541-12020-01-31C16284748780-19d75b9d0-5dc7-f424-e053-dadaa90a57ce48fa4cda-2a3f-4e15-b626-673100b4f923

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BELLIS PERENNISACTIVE INGREDIENT2HU33I03UYBELLIS PERENNIS PELLET [HOMEOLAB USA INC.]1
BELLIS PERENNISACTIVE MOIETY2HU33I03UYBELLIS PERENNIS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GBELLIS PERENNIS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554BELLIS PERENNIS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6541BELLIS PERENNIS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_48fa4cda-2a3f-4e15-b626-673100b4f923.zip