Active Ingredient
Sodium Chloride, 0.65%
Saline Nasal
FDA Label NDC 23558-0569
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lee Pharmaceuticals for the product Saline Nasal (NDC 23558-0569). 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, keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Moisturizer
Uses
For dry nasal membranes
Warnings
Do not use if seal is broken or missing.
Keep Out Of Reach Of Children
The use of this dispenser by more than one person may spread infection.
Directions
- Squeeze twice in each nostril as needed
- Upright delivers a spray, horizontally a stream, upside down a drop
Inactive Ingredients
Benzalkonium chloride, Disodium phosphate, Phenylcarbinol, Monosodium phosphate, Water
* Please review the disclaimer below.
