AKUTUR

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
AKUTUR
Generic name
BENZOIC ACID, NITRIC ACID, APIS MELLIFERA, LYTTA VESICATORIA, POPULUS TREMULOIDES BARK, ANEMONE PRATENSIS FLOWERING TOP, GINGER, AND SOLIDAGO VIRGAUREA FLOWERING TOP
Manufacturer
PEKANA Nautrheilmittel GmbH
Product type
HUMAN OTC DRUG
SPL set ID
7facf36e-c26e-4bc3-a4c1-74e9409f2535
SPL ID
4d19cb5d-3526-4bd8-af97-8ace1615350b
Version
2
Effective date
2023-01-11
Source export date
2026-10-30
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/2026-10-30/e37bebe0ee356110e46fe9b102632217cd5fd64caa93a64cf6ef0d92a0bfdb4c/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 18:52:24
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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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. Protect from light and heat. Tamper Evident Do not use this product if tamper evident strip is broken or removed from base of cap.

Reported adverse events (FAERS/openFDA)#

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