Nasoxinspray
FDA Label NDC 70508-1601
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Friana Llc for the product Nasoxinspray (NDC 70508-1601). 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 package label.principal display panel, otc - active ingredient, otc - keep out of reach of children, otc - purpose, indications & usage, warnings, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Active Ingredient
Sodium Chloride (NaCl 0.95%, Sea salts 1.2%, other salts 0.25%)
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Otc - Purpose
Moisturizes nasal passages
Indications & Usage
for dry nasal membranes
nasal congestion
runny nose
sneezing
itchy nose
irritation
Warnings
Do not use if seal is broken or missing.
The use of this dispenser by more than one person may spread infection.
If pregnant or breast-feeding, or when using on children younger than 4 years of age, consult a health professional.
Dosage & Administration
Squeeze twice in each nostril as needed
Upright delivers a spray, horizontally a stream, upside down a drop
Inactive Ingredient
Purified water
Sodium Oxychlorite 0.04%
* Please review the disclaimer below.
