Active Ingredient
(in each spray)
Triamcinolone acetonide
55 mg (glucocorticoid)
The following Structured Product Label (SPL) was submitted to the FDA by A-s Medication Solutions for the product Nasacort (NDC 50090-1444). 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, do not use, ask a doctor before use if you, when using this product, stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
(in each spray)
Triamcinolone acetonide
55 mg (glucocorticoid)
Allergy symptom reliever
temporarily relieves these symptoms of hay fever or other upper
respiratory allergies:
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center right away.
Read insert (inside package) on how to:
| ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER | |
| adults and children 12 years of age and older |
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| CHILDREN 2 TO UNDER 12 YEARS OF AGE | |
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| children 6 to under 12 years of age |
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| children 2 to under 6 years of age |
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| children under 2 years of age |
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benzalkonium chloride, carboxymethylcellulose sodium, dextrose, edetate disodium, hydrochloric acid or sodium hydroxide (for pH adjustment), microcrystalline cellulose, polysorbate 80, purified water
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