Ruta graveolens 6C

Product NDC
69152-1174
11-digit product format
691521174
Labeler code
69152
Product ID
69152-1174_2f410172-24cb-4c65-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
Ruta graveolens
Dosage form
PELLET
Route
ORAL
Labeler
Paramesh Banerji Life Sciences LLC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-05-12
Marketing end
0000-00-00
Substance
RUTA GRAVEOLENS FLOWERING TOP OIL
Active strength
6 [hp_C]/1
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
69152-1174-12020-01-31C16284748780-19d75b9d0-ce50-f424-e053-dadaa90a57ce15e12b46-511c-1a4b-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69152-1174-1Ruta graveolens 6C96 in 1 BOTTLEPELLET964

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69152-1174RUTA GRAVEOLENS 6C (RUTA GRAVEOLENS) PELLET [PARAMESH BANERJI LIFE SCIENCES LLC]4Legacy NDC, 1 package rows20160330_15e12b46-511c-1a4b-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
69152-1174-16915211740196 in 1 BOTTLEHistorical