FDA Label for Hypertonic Saline Solution Sodium Chloride

The following document was submitted to the FDA by the labeler of this product Naveh Pharma (1996) Ltd. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

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

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