Hypertonic Saline Solution Sodium Chloride Liquid
FDA Label NDC 85202-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Naveh Pharma (1996) Ltd for the product Hypertonic Saline Solution Sodium Chloride (NDC 85202-001). 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 drug facts, active ingredient, purpose, uses:, wornings, do not use, directions, inactive ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Sodium Chloride 3%

Purpose

Moisturizer

Uses:

For dry nasal membranes

Wornings

  • NOT FOR INFECTION
  • Only use sealed vials do not use if vial is broken or already open

Do Not Use

  • after expiration date 
  • Discontinue if you experience any adverse reaction and call your physician

Directions

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

Inactive Ingredients:

USP Water

Package Labeling:

Label2 (Label2)

Label2 (Label2)

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