SALINE NASAL

SALINE NASAL is an FDA-registered drug product whose active ingredient is SODIUM CHLORIDE. It is labelled by ALAINA HEALTHCARE PRIVATE LIMITED taken by nasal and marketed as a human otc drug product. Identifiers on file: NDC 73492-281, application M022, label effective 20260707. It is one of 73 FDA drug label records sharing the active ingredient SODIUM CHLORIDE. 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 SODIUM CHLORIDE are most often described in connection with: nasal passages, provides moisture, helps relieve, dry irritated, due colds, air pollution, decongestants steroidal. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses provides moisture to dry nasal passages helps relieve dry, irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel, and use of decongestants/steroidal sprays.

Directions The use of this dispenser by more than one person may spread infection. Hold bottle upright for spray, horizontally for stream, and upside down for drop. For children and adults, squeeze bottle twice in each nostril, as often as needed, or as directed by doctor. For infants, use drop application.

Warnings If pregnant or breast feeding , ask a health professional before use.

FDA lists 73 drug label records with SODIUM CHLORIDE 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.

5 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is SALINE NASAL used for?
Uses provides moisture to dry nasal passages helps relieve dry, irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel, and use of decongestants/steroidal sprays.

Who makes SALINE NASAL?
ALAINA HEALTHCARE PRIVATE LIMITED is the labeler of record for SALINE NASAL. 73 FDA label records share the active ingredient SODIUM CHLORIDE, 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 SALINE NASAL 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 SALINE NASAL 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 SODIUM CHLORIDE?
Yes. 73 FDA drug label records list SODIUM CHLORIDE 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 SALINE NASAL been recalled?
5 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.