Active Ingredient Purpose
Oxymetazoline Hydrochloride - 0.05% Nazal Decongestant
Maximum Strenth Nasal
FDA Label NDC 0363-7003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Walgreens for the product Maximum Strenth Nasal (NDC 0363-7003). 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, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
For the temporary relief of nasal congestion due to the common cold, hay fever or other upper respiratory allergies.
Warnings
Do not use this product if person has heart disease, high blood pressure, thyroid disease, diabetes, or if adult has difficulty in urination due to enlargement of the prostate gland unless directed by a doctor.
When using this product
Do not exceed recommended dosage
Do not use this product for more than 3 days. Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen. If symptoms persist, consult a doctor.This product may cause temporary discomfort such as burning, stinging, sneezing, or an increase in nasal discharge. The use of this container by more than one person may spread infection.
Directions
Adults and children 6 to under 12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more often than every 10 to 12 hours. Do not exceed 2 doses in any 24-hour period. Children under 6 years of age: consult a doctor.
Inactive Ingredients
Benzalkonium Chloride
Camphor
Disodium EDTA
Eucalyptol
Glycine
Menthol
Polysorbate 80
Propylene Glycol
Sodium Chloride
Sodium Hydroxide
Water
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