Active Ingredient (In Each Spray)
Triamcinolone acetonide 55 mcg (glucocorticoid)
The following Structured Product Label (SPL) was submitted to the FDA by Cardinal Health 110, Llc. Dba Leader for the product Triamcinolone Acetonide (NDC 70000-0702). 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 (in each spray), purpose, uses, warnings, do not use, ask a doctor before use if you, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Triamcinolone acetonide 55 mcg (glucocorticoid)
Allergy symptom reliever
Temporarily relieves these symptoms of hey 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 | |
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| 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 solution (50% W/V) carboxymethylcellulose sodium, dextrose monohydrate, edetate disodium dihydrate, hydrochloric acid, microcrystalline cellulose, polysorbate 80 purified water & sodium hydroxide
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