Hypertonic Saline Liquid
FDA Label NDC 85202-000

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 (NDC 85202-000). 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 ingredients, purpose, inactive ingredients, uses:, wornings, do not use, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredients

Sodium Chloride 7%

Purpose

Moisturizer

Inactive Ingredients

Water

Uses:

For dry nasal membranes

Wornings

  • Do not store above C25°

Do Not Use

  • use jointly with other drugs unlessfirst checking with your dcotor
  • Do not use after expiration date
  • Discontinue if you experience any adverse reaction and call your physician
  • NOT FOR INJECTION 
  • Only use sealed vials - do not use if vial is broken or already open

Directions

  • For dry Nasal Membranes apply as often as needed.

Package Labeling:

Label (Label)

Label (Label)

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