Otc - Active Ingredient
Active Ingredient Purpose
Sodium chloride 0.65%................................Moisturizer
Family Care Premium Saline Nasal
FDA Label NDC 65923-557
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by United Exchange Corp for the product Family Care Premium Saline Nasal (NDC 65923-557). 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 otc - active ingredient, otc - purpose, warnings, otc - keep out of reach of children, otc - do not use, indications & usage, inactive ingredient, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Uses
- For dry nasal membranes
Warnings
Warnings
For external use only
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Otc - Do Not Use
The use of this dispenser by more than one person may spread infection
Indications & Usage
Directions
- squeeze twice in each nostril as needed
- upright delivers a spray, horizontally a stream, upside down a drop
Inactive Ingredient
Inactive Ingredeints
Benzalkonium chloride, dibasic sodium phosphate, monobasic sodium, phosphate, purified water, sorbitol solution
Dosage & Administration
Distributed by:
United Exchange Corp.
17211 Valley View Ave.
Cerritos, CA 90703 USA
Package Label.Principal Display Panel
Image Description (Pa 00557.02 Fc Premsalinenasalspry Lb Ol)
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