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Saline drug information

SALINE NASAL SPRAY
Dynarex Corporation · NASAL

Product NDC: 67777-310

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameSALINE NASAL SPRAY
Labeler / manufacturerDynarex Corporation
RouteNASAL
Drug classDrug class not supplied in source label
Product NDC67777-310
Label effective date2026-08-25

Official product label reference

Saline — Dynarex Corporation

This page contains 11 source sections for SALINE NASAL SPRAY, nasal route. Label set 3247ae7d-554f-baab-e063-6294a90aa3ec, version 2.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Use(s) Moisturizes dry, irritated nasal passages due to: • Colds • Dry air • Smoke • Air travel • Allergies

Purpose

Purpose Restores Moisture
Dosage and administration — label text
Directions • Hold bottle upright and squeeze firmly for spray. • Hold bottle upside down and squeeze gently for a drop. • Use as often as needed or as directed by a physician. • Wipe nozzle-tip clean after each use.
Warnings
Warnings • For Nasal use only • The use of this dispenser by more than one person may spread infection. Do not use • In the eyes. If contact occurs flush with copious amounts of water • For mouth dryness Ask a doctor before use if You are pregnant or breast feeding. Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Active ingredient
Active Ingredient Sodium Chloride 0.65%
Do not use
Do not use • In the eyes. If contact occurs flush with copious amounts of water • For mouth dryness
Ask a doctor before use
Ask a doctor before use if You are pregnant or breast feeding.
Child safety
Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Other safety information
Other Information • Store at room temperature between 15°-30°C (59°-86°F) • Tamper evident. Do not use if seal is torn, cut, or opened.
Inactive ingredient
Inactive Ingredients Benzalkonium Chloride, Benzyl Alcohol, Disodium Phosphate, Sodium Phosphate Monobasic Anhydrous, Water
Questions
Questions? 1-888-396-2739 Monday - Friday 9AM - 5PM EST

Official sources and product identifiers

Substances listed: SODIUM CHLORIDE

RxNorm identifiers: 707251

Package NDC codes

67777-310-01, 67777-310-02, 67777-310-03, 67777-310-04

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.