FDA.reportPublic FDA data

EUPHRASIA OFFICINALIS

Product NDC
60512-1018
11-digit product format
605121018
Labeler code
60512
Product ID
60512-1018_acb70833-8e89-4948-b3e2-9612c061435d
Type
HUMAN OTC DRUG
Nonproprietary name
EUPHRASIA OFFICINALIS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2013-11-18
Marketing end
0000-00-00
Substance
EUPHRASIA STRICTA
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
60512-1018-12025-12-28C16284748780-19d75b9d0-4f8d-f424-e053-dadaa90a57ce19f4ecb6-4f4f-46f1-b0eb-7f415a06584c
60512-1018-12020-01-31C16284748780-19d75b9d0-4f8d-f424-e053-dadaa90a57ce19f4ecb6-4f4f-46f1-b0eb-7f415a06584c

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
EUPHRASIA STRICTAACTIVE INGREDIENTC9642I91WLEUPHRASIA OFFICINALIS PELLET [HOMEOLAB USA INC.]1
EUPHRASIA STRICTAACTIVE MOIETYC9642I91WLEUPHRASIA OFFICINALIS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GEUPHRASIA OFFICINALIS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554EUPHRASIA OFFICINALIS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1018EUPHRASIA OFFICINALIS PELLET [HOMEOLAB USA INC.]1Legacy NDC20140426_19f4ecb6-4f4f-46f1-b0eb-7f415a06584c.zip