FEBRIPLEX

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
FEBRIPLEX
Generic name
ACONITUM NAPELLUS, ARNICA MONTANA, BELLADONNA, EUPATORIUM PERFOLIATUM, GELSEMIUM SEMPERVIRENS, MERCURIUS SOLUBILIS, RHUS TOXICODENDRON
Manufacturer
Seroyal USA
Product type
HUMAN OTC DRUG
SPL set ID
52e1f6ff-f4b9-693a-e054-00144ff8d46c
SPL ID
eceb2ab1-7e67-dd8c-e053-2a95a90aa848
Version
4
Effective date
2022-11-07
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:28:18
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

Warnings Stop use and ask a doctor if symptoms continue to persist after three days of use or are accompanied by a fever. Do not use if you have ever had an allergic reaction to this product or any of its ingredients. If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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