FDA Label for Nekvnro Original Nasal
View Indications, Usage & Precautions
Nekvnro Original Nasal Product Label
The following document was submitted to the FDA by the labeler of this product Jiangxi Hemei Pharmaceutical Co., Ltd. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Active Ingredient
Naphazoline HCL 0.05%.
Purpose
Nasal Decongestant
Use
temporarily relieves
*nasal congestion due to a cold, hay fever, or other upper respiratory allergies
*sinus congestion and pressure
Warnings
Ask a doctor before use if you have
·heart disease
·high blood pressure
·thyroid disease
·diabetes
·trouble urinating due to enlarged prostate gland
Do Not Use
children under 2 years
When Using
·do not exceed recommended dosage
·do not use this product for more than 7 days. Use only as directed. Frequent or prolonged use may cause nasal congestion to recur or worsen
·temporary discomfort such as burning, stinging,sneezing, or increased nasal discharge may occur
·use ofthis container by more than one person mayspread infection
Stop Use
symptoms persist.
Ask Doctor
children 2 to under 6 years.
Keep Oot Of Reach Of Children
If swallowed,get medical help or contact a Poison Control Center right away
Directions
adults & children 6 yrs. & older (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 24 hours.
Other Information
do not exceed 25°C
Inactive Ingredients
borneol, Camphor,glycerin,Glycerol, menthol, propylene ,glycol, etc.
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