Drosera

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
Drosera
Generic name
DROSERA ROTUNDIFOLIA
Manufacturer
Boiron
Product type
HUMAN OTC DRUG
SPL set ID
858e147c-b336-8392-e053-2991aa0a7749
SPL ID
0a0c9e7f-6ddd-b628-e063-6394a90a5916
Version
2
Effective date
2023-11-13
Source export date
2026-10-12
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/f40eac55ff4c5d55c3d8bbc5766ea7e21e4196960cfb4703b96a406b491c0cd5/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:30:46
Harmonized routes table
Harmonized routes
ORAL

Reported adverse events (FAERS/openFDA)#

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