SinuFix

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
SinuFix
Generic name
THUJA OCCIDENTALIS, ANTIMONIUM TARTARICUM, KALI BICHROMICUM, MERCURIUS IODATUS RUBER, SPONGIA TOSTA, HEPAR SULPHURIS CALCAREUM
Manufacturer
NaturalCare
Product type
HUMAN OTC DRUG
SPL set ID
3e2346e7-55a1-416e-b2ef-04d43e40d67f
SPL ID
fbd27f97-5014-489e-8d3a-1475247f8b4d
Version
1
Effective date
2026-04-22
Source export date
2026-09-28
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/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:38:14
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 worsen or persist for more than 5 days ■ new symptoms appear If pregnant or breast-feeding, 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. Do not use if tamper evident seal is missing or open. ■ Store at room temperature (65-80ºF)

Reported adverse events (FAERS/openFDA)#

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