BHI Sinus

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
BHI Sinus
Generic name
EUPHORBIA RESINIFERA RESIN, GOLDENSEAL, POTASSIUM DICHROMATE, POTASSIUM IODIDE, PHOSPHORUS, PULSATILLA VULGARIS, AND THUJA OCCIDENTALIS LEAFY TWIG
Manufacturer
MediNatura Inc
Product type
HUMAN OTC DRUG
SPL set ID
cb11ccaf-7569-4cf3-8064-811c7db11001
SPL ID
fe477719-75f6-4273-9a61-5bc8ef7bdb47
Version
4
Effective date
2022-08-08
Source export date
2026-10-30
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-30/9dea423b9e87a781c152bc6e136923fb91acb0732a7a0ec0d2a51142148f160c/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 18:43:52
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if known sensitivity to BHI Sinus or any of its ingredients exists.

Reported adverse events (FAERS/openFDA)#

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