Active Ingredient
Sodium Chloride 0.65%
Personal Care Saline Nasal Spray
FDA Label NDC 20276-439
11 label sections · Submitted to the FDA by Delta Brands Inc. · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Delta Brands Inc. for the product Personal Care Saline Nasal (NDC 20276-439). 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, do not use, ask a doctor before use if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Nasal Moisturizer
Uses
Moisturizes dry, irritated nasal passages due to: ■ Colds ■Dry air ■Smoke ■Air travel ■Allergies
Warnings
■ For nasal use only ■ The use of this dispenser by more than one person may spread infection
Do Not Use
■ in the eyes ■ for mouth dryness ■ if printed neckband is broken or missing
Ask A Doctor Before Use If
If you are pregnant or breastfeeding
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away
Directions
Squeeze twice in each nostril as needed or as directed by physician. For children 3 years old and younger consult a physician before use. For infants , use drop application. Hold bottle upright for spray, horizontally for stream, and upside down for drop.
Inactive Ingredients
benzalkonium chloride, benzyl alcohol, disodium phosphate, sodium phosphate, water
Questions Or Comments?
1-866-467-2748
*This product is not manufactured or distributed by Valeant Pharmaceuticals North America LLC, sodium phosphate monobasic.
Package Label
PCSalineSpry
Saline Spray Label (Pcsalinespry)
* Please review the disclaimer below.
