FDA.reportPublic FDA data

ECHINACEA PURPUREA

Product NDC
60512-6651
11-digit product format
605126651
Labeler code
60512
Product ID
60512-6651_72bfae31-b7e6-4ca2-87d4-d7e54efa9b18
Type
HUMAN OTC DRUG
Nonproprietary name
ECHINACEA PURPUREA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-11-18
Marketing end
0000-00-00
Substance
ECHINACEA PURPUREA
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
60512-6651-12025-12-30C16284748780-19d75b9cf-f7ac-f424-e053-dadaa90a57ce6251215d-19d1-4736-88de-0f7e20d2f13d
60512-6651-12020-01-31C16284748780-19d75b9cf-f7ac-f424-e053-dadaa90a57ce6251215d-19d1-4736-88de-0f7e20d2f13d

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ECHINACEA PURPUREAACTIVE INGREDIENTQI7G114Y98ECHINACEA PURPUREA PELLET [HOMEOLAB USA INC.]1
ECHINACEA PURPUREAACTIVE MOIETYQI7G114Y98ECHINACEA PURPUREA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GECHINACEA PURPUREA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ECHINACEA PURPUREA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6651ECHINACEA PURPUREA PELLET [HOMEOLAB USA INC.]1Legacy NDC20140514_6251215d-19d1-4736-88de-0f7e20d2f13d.zip