Hypertonic Saline Solution Sodium Chloride

SODIUM CHLORIDE TOPICAL HUMAN OTC DRUG

Hypertonic Saline Solution Sodium Chloride is an FDA drug label for the active ingredient SODIUM CHLORIDE manufactured by NAVEH PHARMA (1996) LTD administered by TOPICAL. 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 20260730.

Generic name
SODIUM CHLORIDE
Manufacturer
NAVEH PHARMA (1996) LTD
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
85202-001
Application
N/A
Label effective
20260730

About this product

Hypertonic Saline Solution Sodium Chloride is an FDA-registered drug product whose active ingredient is SODIUM CHLORIDE. It is labelled by NAVEH PHARMA (1996) LTD taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85202-001, label effective 20260730. 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.

What it is used for

Across FDA labelling, products containing SODIUM CHLORIDE are most often described in connection with: dry nasal. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient Sodium Chloride 3% Purpose Moisturizer

Indications & Usage

Uses: For dry nasal membranes

Dosage & Administration

Directions Apply solution with fingers or swab directly into nose Apply 2-3 rounds per nostril to sanitize and moisturize passages

Warnings

Wornings NOT FOR INFECTION Only use sealed vials do not use if vial is broken or already open Keep out of reach of children Do not use after expiration date Discontinue if you experience any adverse reaction and call your physician

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How products containing SODIUM CHLORIDE compare

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.

Dosage formProductsManufacturerProducts
— — Boiron 14
— — Baxter Healthcare Corporation 9
— — Fresenius Kabi USA, LLC 8
— — ASCENT CONSUMER PRODUCTS, INC 3
— — B. Braun Medical Inc. 3

Frequently asked questions

What is Hypertonic Saline Solution Sodium Chloride used for?
Uses: For dry nasal membranes

Who makes Hypertonic Saline Solution Sodium Chloride?
NAVEH PHARMA (1996) LTD is the labeler of record for Hypertonic Saline Solution Sodium Chloride. 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 Hypertonic Saline Solution Sodium Chloride come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Hypertonic Saline Solution Sodium Chloride 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 Hypertonic Saline Solution Sodium Chloride 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.