Active Ingredient Purpose
Oxymetazoline Hydrochloride 0.05% Nasal decongestant
The following Structured Product Label (SPL) was submitted to the FDA by Rite Aid for the product Nasal Relief (NDC 11822-1230). 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, warnings, when using this product, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Oxymetazoline Hydrochloride 0.05% Nasal decongestant
Warnings
Do not use this product if you have heart disease • high
blood pressure • thyroid disease
• diabetes • or difficulty in urination due to enlargement of
the prostate gland
• Do not exceed recommended
dosage. • 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. • Do not use for more than 3 days. Use only as
directed. • Frequent or prolonged use may cause nasal
congestion to recur or worsen.
Before using the first time, remove the protective cap from the tip and prime pump by depressing pump firmly several times.
To spray, hold bottle with thumb at base and nozzle between first and second fingers. Without tilting head, insert nozzle into nostril. Fully depress rim with a firm, even stroke and sniff deeply. Wipe nozzle clean after use. • adults and children 6 to under12 years of age (with adult supervision): 2 or 3 sprays in each nostril not more often than every 1 0 to 1 2 hours. Do not exceed 2 doses within any 24-hour period • children under 6 years of age: consult a doctor
Benzalkonium Chloride
Chlorhexidine Gluconate
Citric Acid
Disodium EDTA
Fragrance
Purified Water
Sodium Citrate
Sodium Hydroxide
Tyloxapol
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