FDA.reportPublic FDA data

ARTEMISIA VULGARIS

Product NDC
60512-6516
11-digit product format
605126516
Labeler code
60512
Product ID
60512-6516_cce6f006-bc05-4f02-81c9-d5ffc2367a1a
Type
HUMAN OTC DRUG
Nonproprietary name
ARTEMISIA VULGARIS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ARTEMISIA VULGARIS ROOT
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
60512-6516-12025-12-29C16284748780-19d75b9d0-8a2b-f424-e053-dadaa90a57ce74aa3999-8b10-4e95-9ccd-9897aa66f027
60512-6516-12020-01-31C16284748780-19d75b9d0-8a2b-f424-e053-dadaa90a57ce74aa3999-8b10-4e95-9ccd-9897aa66f027

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARTEMISIA VULGARIS ROOTACTIVE INGREDIENT32MP823R8SARTEMISIA VULGARIS PELLET [HOMEOLAB USA INC.]1
ARTEMISIA VULGARIS ROOTACTIVE MOIETY32MP823R8SARTEMISIA VULGARIS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GARTEMISIA VULGARIS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ARTEMISIA VULGARIS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6516ARTEMISIA VULGARIS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131030_74aa3999-8b10-4e95-9ccd-9897aa66f027.zip