Home NDC 76472-1160 Ruta Graveolens
Product NDC 76472-1160
11-digit product format 764721160
Labeler code 76472
Product ID 76472-1160_10316818-6a96-faa1-e063-6294a90aa804
Type HUMAN OTC DRUG
Nonproprietary name RUTA GRAVEOLENS
Dosage form PELLET
Route SUBLINGUAL
Labeler SEVENE USA
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2011-11-30
Substance RUTA GRAVEOLENS FLOWERING TOP
Active strength 30 [hp_C]/1
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Ruta Graveolens
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength RUTA GRAVEOLENS FLOWERING TOP 30 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination N94C2U587S Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 76472-1160-1 Ruta Graveolens 80 in 1 CYLINDER PELLET 80 21
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 76472-1160 RUTA GRAVEOLENS PELLET [SEVENE USA] 21 Current NDC, Legacy NDC, 1 package rows 20240131_a92b2c14-05a3-4d11-908e-c32325b06eb4.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 76472-1160-1 76472116001 80 PELLET in 1 CYLINDER (76472-1160-1) 80 pellet 2011-11-30 0000-00-00 No No Current