B03 Sinus Relief

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: B03 Sinus Relief
Generic name: ALLIUM CEPA, CALCAREA IODATA, CALCAREA SULPHURICA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, EUPHORBIUM OFFICINARUM, HEPAR SULPHURIS CALCAREUM, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, KALI MURIATICUM, KALI SULPHURICUM, LAC DEFLORATUM, LUFFA OPERCULATA, MERCURIUS SULPHURATUS RUBER, PHOSPHORUS, PULSATILLA VULGARIS, SACCHARUM LACTIS, THUJA OCCIDENTALIS
Manufacturer: Apex Energetics Inc.
Product type: HUMAN OTC DRUG
SPL set ID: bad83f77-e9ae-7118-e053-2a95a90aa737
SPL ID: 47428a99-4994-566c-e063-6294a90a939b
Version: 4
Effective date: 2025-12-31
Source export date: 2026-09-28
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/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:26:36

Harmonized routes table
Harmonized routes
SUBLINGUAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		B03 Sinus Relief	openfda.brand_name
generic name		ALLIUM CEPA, CALCAREA IODATA, CALCAREA SULPHURICA, ECHINACEA ANGUSTIFOLIA, ECHINACEA PURPUREA, EUPHORBIUM OFFICINARUM, HEPAR SULPHURIS CALCAREUM, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, KALI MURIATICUM, KALI SULPHURICUM, LAC DEFLORATUM, LUFFA OPERCULATA, MERCURIUS SULPHURATUS RUBER, PHOSPHORUS, PULSATILLA VULGARIS, SACCHARUM LACTIS, THUJA OCCIDENTALIS	openfda.generic_name
manufacturer name		Apex Energetics Inc.	openfda.manufacturer_name
ndc	package	63479-0203-1	openfda.package_ndc
ndc	product	63479-0203	openfda.product_ndc
ndc11	package	63479020301	derived:openfda.package_ndc
spl id		47428a99-4994-566c-e063-6294a90a939b	id
spl set id		bad83f77-e9ae-7118-e053-2a95a90aa737	set_id
unii		27YLU75U4W	openfda.unii
unii		E934B3V59H	openfda.unii
unii		6A001Y4M5A	openfda.unii
unii		3POA0Q644U	openfda.unii
unii		1TI1O9028K	openfda.unii
unii		1NT28V9397	openfda.unii
unii		1K573LC5TV	openfda.unii
unii		VB06AV5US8	openfda.unii
unii		C4MO6809HU	openfda.unii
unii		660YQ98I10	openfda.unii
unii		492225Q21H	openfda.unii
unii		ZW3Z11D0JV	openfda.unii
unii		QI7G114Y98	openfda.unii
unii		T4423S18FM	openfda.unii
unii		J2B2A4N98G	openfda.unii
unii		8EKI9QEE2H	openfda.unii
unii		ZI0T668SF1	openfda.unii
unii		I76KB35JEV	openfda.unii
unii		1MBW07J51Q	openfda.unii

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: If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if sinus congestion, coughing, fatigue, nasal discharge, frontal headache, muscle aches, or other symptoms do not improve within 7 days or are accompanied by fever.

Reported adverse events (FAERS/openFDA)#

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