Hendel Sinus Relief
Hendel Sinus Relief is an FDA drug label for the active ingredient ECHINACEA PURPUREA, ANEMONE PULSATILLA, EUPATORIUM PERFOLIATUM FLOWERING, GOLDENSEAL, POTASSDICHROMATE, LUFFA OPERCULATA FRUIT, POTASSIUM IODIDE, CALCIUM SULFIDE AND MERCURIC SULFIDE manufactured by MediNatura Inc administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20220818.
- Generic name
- ECHINACEA PURPUREA, ANEMONE PULSATILLA, EUPATORIUM PERFOLIATUM FLOWERING, GOLDENSEAL, POTASSDICHROMATE, LUFFA OPERCULATA FRUIT, POTASSIUM IODIDE, CALCIUM SULFIDE AND MERCURIC SULFIDE
- Manufacturer
- MediNatura Inc
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 62795-1134
- Application
- N/A
- Label effective
- 20220818
About this product
Hendel Sinus Relief is an FDA-registered drug product whose active ingredient is ECHINACEA PURPUREA, ANEMONE PULSATILLA, EUPATORIUM PERFOLIATUM FLOWERING, GOLDENSEAL, POTASSDICHROMATE, LUFFA OPERCULATA FRUIT, POTASSIUM IODIDE, CALCIUM SULFIDE AND MERCURIC SULFIDE. It is labelled by MediNatura Inc taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 62795-1134, label effective 20220818. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing ECHINACEA PURPUREA, ANEMONE PULSATILLA, EUPATORIUM PERFOLIATUM FLOWERING, GOLDENSEAL, POTASSDICHROMATE, LUFFA OPERCULATA FRUIT, POTASSIUM IODIDE, CALCIUM SULFIDE AND MERCURIC SULFIDE are most often described in connection with: sinus pressure. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
USES • Sinus Pressure & Headache
Dosage & Administration
DIRECTIONS Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician
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 sensitivity to Sinus Relief or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.
Frequently asked questions
What is Hendel Sinus Relief used for?
USES • Sinus Pressure & Headache
Who makes Hendel Sinus Relief?
MediNatura Inc is the labeler of record for Hendel Sinus Relief.
What form does Hendel Sinus Relief come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Hendel Sinus Relief prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Hendel Sinus Relief been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.