Artemisia vulgaris 1X

Product NDC
69152-1574
11-digit product format
691521574
Labeler code
69152
Product ID
69152-1574_1695b8e1-79c3-5975-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
Artemisia vulgaris
Dosage form
LIQUID
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-05-09
Marketing end
0000-00-00
Substance
ARTEMISIA VULGARIS ROOT
Active strength
1 [hp_X]/8mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69152-1574-12020-01-31C16284748780-19d75b9d0-4507-f424-e053-dadaa90a57ce15a4d71a-e2e9-6395-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1574-1Artemisia vulgaris 1X8 mL in 1 BOTTLE, DROPPERLIQUID82

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1574ARTEMISIA VULGARIS 1X (ARTEMISIA VULGARIS) LIQUID [PARAMESH BANERJI LIFE SCIENCES LLC]2Legacy NDC, 1 package rows20150521_15a4d71a-e2e9-6395-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69152-1574-1691521574018 mL in 1 BOTTLE, DROPPER8 mlHistorical