RUTA GRAVEOLENS 200ck

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
RUTA GRAVEOLENS 200ck
Generic name
RUTA GRAVEOLENS
Manufacturer
SEVENE USA
Product type
HUMAN OTC DRUG
SPL set ID
cf898a11-a78e-342d-e053-2995a90a5b05
SPL ID
2dcc6b2e-b3d5-e17b-e063-6294a90a2fd2
Version
4
Effective date
2025-02-10
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:53:57
Harmonized routes table
Harmonized routes
SUBLINGUAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS Stop use and ask a physician if symptoms persist for more than 3 days or worsen.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.