FDA.reportPublic FDA data

ECHINACEA ANGUSTIFOLIA

Product NDC
60512-6650
11-digit product format
605126650
Labeler code
60512
Product ID
60512-6650_efb05de7-53bb-4623-8dc3-8cdb296e2087
Type
HUMAN OTC DRUG
Nonproprietary name
ECHINACEA ANGUSTIFOLIA
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 ANGUSTIFOLIA
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
60512-6650-12025-12-26C16284748780-19d75b9d0-d291-f424-e053-dadaa90a57cee7ed2ebd-d857-4ffc-978d-e88f157e80d0
60512-6650-12020-01-31C16284748780-19d75b9d0-d291-f424-e053-dadaa90a57cee7ed2ebd-d857-4ffc-978d-e88f157e80d0

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ECHINACEA ANGUSTIFOLIAACTIVE INGREDIENTVB06AV5US8ECHINACEA ANGUSTIFOLIA PELLET [HOMEOLAB USA INC.]1
ECHINACEA ANGUSTIFOLIAACTIVE MOIETYVB06AV5US8ECHINACEA ANGUSTIFOLIA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GECHINACEA ANGUSTIFOLIA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ECHINACEA ANGUSTIFOLIA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6650ECHINACEA ANGUSTIFOLIA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131125_e7ed2ebd-d857-4ffc-978d-e88f157e80d0.zip