NebuClear MD Saline

NebuClear MD Saline is an FDA-registered drug product whose active ingredient is NEBUCLEAR MD SALINE. It is labelled by Blue Echo Care LLC taken by nasal and marketed as a human otc drug product. Identifiers on file: NDC 73117-522, application M022, label effective 20260630. It is one of 3 FDA drug label records sharing the active ingredient NEBUCLEAR MD SALINE. 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.

Across FDA labelling, products containing NEBUCLEAR MD SALINE are most often described in connection with: moisturizing dry, nasal passages, dryness associated, colds allergies. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Moisturizing dry nasal passages and relieves nasal dryness associated with colds, allergies, sinusitis or dry air.

Directions Adults and children: Administer into nasal passageway as often as needed or as directed by a physician. For infants, apply using drops. Follow the instructions provided with the delivery device for proper administration. To help prevent the spread of infection, do not share the dispenser or delivery device with others.

Warnings Not for Injection Do not use after expiration date Discontinue if you experience any adverse reactions and call your physician Only use sealed vials Do not use if vial is broken

FDA lists 3 drug label records with NEBUCLEAR MD SALINE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is NebuClear MD Saline used for?
Uses Moisturizing dry nasal passages and relieves nasal dryness associated with colds, allergies, sinusitis or dry air.

Who makes NebuClear MD Saline?
Blue Echo Care LLC is the labeler of record for NebuClear MD Saline. 3 FDA label records share the active ingredient NEBUCLEAR MD SALINE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does NebuClear MD Saline come in?
administered by nasal. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is NebuClear MD Saline 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.

Are there other products containing NEBUCLEAR MD SALINE?
Yes. 3 FDA drug label records list NEBUCLEAR MD SALINE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has NebuClear MD Saline 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.