Saline Nasal Spray
FDA Label NDC 73492-281

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Alaina Healthcare Private Limited for the product Saline Nasal (NDC 73492-281). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, directions, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Sodium Chloride 0.65%

Purpose

Moisturizer

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.

Warnings

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

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.

Inactive Ingredients

benzalkonium chloride, disodium hydrogen phosphate anhydrous, purified water, sodium acid phosphate.

Principal Display Panel

Saline Nasal Spray
Sodium Chloride 0.65%
Relieves dry nasal passages
Soothes dry, stuffy noses
Safe for frequent daily use
Compare to active ingredients in OCEAN ®
1.5 FL OZ (44 mL)

"image Description" (Sodium Chloride Nasal Spray 44ml Bottle Label)

"image Description" (Sodium Chloride Nasal Spray 44ml Bottle Label)

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