CLAUPAREST

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
CLAUPAREST
Generic name
ARANEUS DIADEMATUS, ARNICA MONTANA ROOT, CUPRIC ACETATE, MANDRAGORA OFFICINARUM ROOT, LEAD ACETATE ANHYDROUS, TOBACCO LEAF, MELILOTUS OFFICINALIS TOP, AND RUTA GRAVEOLENS FLOWERING TOP
Manufacturer
PEKANA Naturheilmittel GmbH
Product type
HUMAN OTC DRUG
SPL set ID
d7ac09b0-b2a8-48d0-8f9f-55478cba2a48
SPL ID
7aca5451-c6f8-4820-a3a7-a1820546f734
Version
7
Effective date
2022-12-06
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:46:29
Harmonized routes table
Harmonized routes
ORAL

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

Warning If symptoms persist, contact a licensed practitioner. If you have known sensitivity to any of the ingredients, please consult your licensed practitioner before use. If you are pregnant or nursing a baby, seek the advice of a health care professional before use. Keep out of the reach of children.

Reported adverse events (FAERS/openFDA)#

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