Device - NebuClear MD Hand-held Rubber Bulb Nebulizer
Device - NebuClear MD Hand-held Rubber Bulb Nebulizer is an FDA drug label for the active ingredient DEVICE - HAND-HELD RUBBER BULB NEBULIZER manufactured by Blue Echo Care LLC administered by RESPIRATORY (INHALATION). 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 20260511.
- Generic name
- DEVICE - HAND-HELD RUBBER BULB NEBULIZER
- Manufacturer
- Blue Echo Care LLC
- Product type
- HUMAN OTC DRUG
- Route
- RESPIRATORY (INHALATION)
- Dosage form
- N/A
- NDC
- 73117-509
- Application
- M012
- Label effective
- 20260511
About this product
Device - NebuClear MD Hand-held Rubber Bulb Nebulizer is an FDA-registered drug product whose active ingredient is DEVICE - HAND-HELD RUBBER BULB NEBULIZER. It is labelled by Blue Echo Care LLC taken by respiratory (inhalation) and marketed as a human otc drug product. Identifiers on file: NDC 73117-509, application M012, label effective 20260511. 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 DEVICE - HAND-HELD RUBBER BULB NEBULIZER are most often described in connection with: please consult, otc bronchodilator, drug label. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Indications & Usage
Uses Please consult the use section of the OTC bronchodilator drug label approved for use with this device.
Dosage & Administration
Directions Connect bulb to solutions cup. Open top of cup, add approved Bronchodilator, close solutions cup. Squeeze bulb vigorously so visible vapor comes from the top. Breathe in slowly until approved Bronchodilator is gone. Disconnect bulb and follow Cleaning Instructions.
Warnings
Warnings Please consult the warnings secton for the OTC bronchodilator drug label before use with this device.
Frequently asked questions
What is Device - NebuClear MD Hand-held Rubber Bulb Nebulizer used for?
Uses Please consult the use section of the OTC bronchodilator drug label approved for use with this device.
Who makes Device - NebuClear MD Hand-held Rubber Bulb Nebulizer?
Blue Echo Care LLC is the labeler of record for Device - NebuClear MD Hand-held Rubber Bulb Nebulizer.
What form does Device - NebuClear MD Hand-held Rubber Bulb Nebulizer come in?
administered by respiratory (inhalation). Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Device - NebuClear MD Hand-held Rubber Bulb Nebulizer 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 Device - NebuClear MD Hand-held Rubber Bulb Nebulizer 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.