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Nazal

Dosage form
LIQUID
Labeler
Sato Pharmaceutical Co., Ltd.
Label updated
2023-12-06
Retrieved
2026-09-07
Active ingredients
NAPHAZOLINE HYDROCHLORIDE
View original label and images on DailyMed ↗
유효 성분

Active ingredients  
Naphazoline hydrochloride 0.05%

성분·작용

Purpose    Nasal decongestant

효능·용도

Uses for the temporary relief of nasal congestion due to the common cold, hay fever, or associated with sinusitis

주의사항

Warnings
For external use only

Label information

Do not use

■for more than 3 days

■in children under 12 years of age because it may cause sedation if swallowed

Label information

Ask a doctor before use if you have

■heart disease

■high blood pressure

■thyroid disease ■diabetes

■difficulty in urination due to enlargement of the prostate gland

Label information

When using this product

■do not exceed recommended dosage

■if 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

■use only as directed

■frequent or prolonged use may cause nasal congestion to recur or worsen

Label information

Stop use and ask a doctor if

■symptoms persist

Label information

If pregnant or breast-feeding, ask a health professional before use.

Label information

Keep our of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center right away.


복용법·사용법

Directions
Adults and children 12 years of age and older - 1 or 2 sprays in each nostril not more often than every 6 hours
Children under 12 years of age -  do not give unless directed by a doctor

Label information

Other information  
■container is filled to proper level for best spray action

첨가제

Inactive ingredients
benzalkonium chloride, citric acid, dibasic potassium phosphate, fragrance, monobasic potassium phosphate, simethicone, sodium chloride, water

포장 표시

nazalcart.jpg

[Image in the official label — see DailyMed source]

DailyMed Set ID: 4d4043f8-5ed3-4027-beb6-687db1308202 · Version 7
NDC: 49873-057