Hendel Sinus Relief

Manufacturer
MediNatura Inc
Effective date
2022-08-18
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 02:18:02

Label at a glance#

ProductHendel Sinus Relief
Active ingredientECHINACEA PURPUREA, ANEMONE PULSATILLA, EUPATORIUM PERFOLIATUM FLOWERING TOP, GOLDENSEAL, POTASSIUM DICHROMATE, LUFFA OPERCULATA FRUIT, POTASSIUM IODIDE, CALCIUM SULFIDE, MERCURIC SULFIDE
Label structure8 sections

Indications and uses

• Sinus Pressure & Headache

Dosage and administration

Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician

Label contents#

Full prescribing information#

WARNINGS

WARNINGS SECTION

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 sensitivity to Sinus Relief or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS

OTC - PURPOSE SECTION

Sinus Relief

INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Each tablet contains equal parts of Echinacea purpurea 3X, Pulsatilla 4X, Eupatorium perfoliatum 6X, Hydrastis canadensis 6X, Kali bichromicum 6X, Luffa operculata 6X, Kali iodatum 8X, Hepar sulphuris calcareum 10X, Mercurius sulphuratus ruber 12X.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Lactose, Magnesium stearate

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician

USES

INDICATIONS & USAGE SECTION

• Sinus Pressure & Headache

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hendel Sinus ReliefHendel Sinus Relief

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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62795-1134-22020-11-04C16284748780-19d75b9d0-f988-f424-e053-dadaa90a57ceHendel Sinus Relief
62795-1134-22020-01-31C16284748780-19d75b9d0-f988-f424-e053-dadaa90a57ceHendel Sinus Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62795-1134-2Hendel Sinus Relief100 in 1 PACKAGETABLET1005

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62795-1134HENDEL SINUS RELIEF (ECHINACEA PURPUREA, ANEMONE PULSATILLA, EUPATORIUM PERFOLIATUM FLOWERING, GOLDENSEAL, POTASSDICHROMATE, LUFFA OPERCULATA FRUIT, POTASSIUM IODIDE, CALCIUM SULFIDE AND MERCURIC SULFIDE) TABLET [MEDINATURA INC]5Current NDC, Legacy NDC, 1 package rows20220820_819425a8-b4ec-4049-95cb-187f6729dde5.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
62795-1134-2EA - Each62795-113493a45b78-64b7-40fc-8c0b-d249d883a60912022-07-06

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62795-113462795-1134-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Hendel Sinus ReliefECHINACEA PURPUREA, ANEMONE PULSATILLA, EUPATORIUM PERFOLIATUM FLOWERING, GOLDENSEAL, POTASSDICHROMATE, LUFFA OPERCULATA FRUIT, POTASSIUM IODIDE, CALCIUM SULFIDE AND MERCURIC SULFIDEMediNatura Inc819425a8-b4ec-4049-95cb-187f6729dde52022-08-18WarningsExact identifier
ndc (package): 62795-1134-2
ndc (product): 62795-1134
ndc11 (package): 62795113402
spl id: e9e1ff34-9e67-47ae-a2f9-335160791be2
spl set id: 819425a8-b4ec-4049-95cb-187f6729dde5

Reported adverse events (FAERS/openFDA)#

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