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CVS Saline drug information

NASAL
CVS PHARMACY · NASAL

Product NDC: 69842-438

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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 nameNASAL
Labeler / manufacturerCVS PHARMACY
RouteNASAL
Drug classDrug class not supplied in source label
Product NDC69842-438
Label effective date2026-08-19

Official product label reference

CVS Saline — CVS PHARMACY

This page contains 9 source sections for NASAL, nasal route. Label set f02c41b0-c78e-41cd-aa4a-2756bbe92087, version 8.

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

Uses provides instant, soothing relief to dry irritated nasal passages due to colds, allergies, dry air, pollution, smoke, air travel and use of decongestants/steroidal sprays.

Purpose

Purpose Moisturizer
Dosage and administration — label text
Directions For children and adults, squeeze bottle twice in each nostril as often as needed or as directed by physician. For infants, use drop application. Hold bottle upright for spray, horizontally for stream, and upside down for drop. The use of this dispenser by more than one person may spread infection.
Warnings
Warnings If pregnant or breast-feeding, ask a healthcare professional before use.
Active ingredient
Drug Facts Active Ingredients Sodium Chloride 0.65%
Child safety
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222
Other safety information
Other Information • store at room temperature
Inactive ingredient
Inactive Ingredients Aloe barbadensis leaf juice (aloe vera gel), benzalkonium chloride, benzyl alcohol, purified water, sodium phosphate dibasic, sodium phosphate monobasic
Questions
Questions or comments? 1-866-467-2748 *This product is not manufactured or distributed by Valeant Pharmaceuticals North America LLC, owners of the registered trademark Ocean®. Distributed by:

Official sources and product identifiers

Substances listed: SODIUM CHLORIDE

RxNorm identifiers: 707251

Package NDC codes

69842-438-30

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.