Label: NASACORT ALLERGY 24HR- triamcinolone acetonide spray, metered

  • NDC Code(s): 41167-5800-1, 41167-5800-2, 41167-5800-3, 41167-5800-5, view more
    41167-5800-6, 41167-5800-7
  • Packager: Chattem, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated February 19, 2024

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  • SPL UNCLASSIFIED SECTION

    Nasacort Allergy 24HR

    Drug Facts

  • Active ingredient

    (in each spray) 

    Triamcinolone acetonide 

    55 mcg (glucocorticoid)

  • Purpose

    Allergy symptom reliever

  • Uses

    temporarily relieves these symptoms of hay fever or other upper
    respiratory allergies:

    • nasal congestion  
    • runny nose  
    • sneezing  
    • itchy nose
  • Warnings

    Do not use

    • in children under 2 years of age
    • if you have ever had an allergic reaction to any of the ingredients

    Ask a doctor before use if you

    • have had recent nose ulcers or nose surgery
    • have had a nose injury that has not healed
    • are using a steroid medicine for asthma, allergies or skin rash
    • have an eye infection
    • have or had glaucoma or cataracts

    When using this product

    • the growth rate of some children may be slower
    • some symptoms may get better on the first day of treatment. It may take up to one week of daily use to feel the most symptom relief.
    • do not share this bottle with anyone else as this may spread germs
    • remember to tell your doctor about all the medicines you take, including this one

    Stop use and ask a doctor if

    • you have, or come into contact with someone who has, chickenpox, measles or tuberculosis
    • you have or develop symptoms of an infection such as a persistent fever
    • you have any change in vision
    • you have severe or frequent nosebleeds

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    In case of overdose, get medical help or contact a Poison Control Center right away.

  • Directions

    Read insert (inside package) on how to:

    • get a new bottle ready (primed) before first use
    • prime bottle again if not used for more than 2 weeks
    • use the spray
    • clean the spray nozzle
     ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER
    adults and children 12
    years of age and older    		 
    • once daily, spray 2 times into each nostril while sniffing gently
    • once your allergy symptoms improve, reduce to 1 spray in each nostril per day
     CHILDREN 2 TO UNDER 12 YEARS OF AGE
     
    • the growth rate of some children may be slower while using this product. Talk to your child’s doctor if your child needs to use the spray for longer than two months a year.
     children 6 to under 12 years of age 
    • an adult should supervise use
    • once daily, spray 1 time into each nostril while sniffing gently
    • if allergy symptoms do not improve, increase to 2 sprays in each nostril per day. Once allergy symptoms improve, reduce to 1 spray in each nostril per day.
     children 2 to under 6 years of age 
    • an adult should supervise use
    • once daily, spray 1 time into each nostril while sniffing gently
     children under 2 years of age 
    • do not use
    • do not use more than directed
    • if you forget a dose, do not double the next dose
    • do not spray into eyes or mouth
    • if allergy symptoms do not improve after one week, stop using and talk to a doctor
    • do not use for the common cold
    • shake well before each use
  • Other information

    • do not use if sealed package is torn or opened
    • keep package and insert. They contain important information.
    • store between 20°- 25°C (68°-77°F)
  • Inactive ingredients

    benzalkonium chloride, carboxymethylcellulose sodium, dextrose, edetate disodium, hydrochloric acid or sodium hydroxide (for pH adjustment), microcrystalline cellulose, polysorbate 80, purified water

  • Questions or comments?

    call toll-free 1-800-633-1610

  • Principal Display Panel

    NDC 41167-5800-3
    Multi-Symptom
    Nasal Allergy Spray
    Nasacort
    Allergy 24HR
    triamcinolone acetonide nasal spray 55 mcg per spray
    allergy symptom reliever
    (glucocorticoid)*
    0.37 fl. oz. (10.8 ml) 60 Sprays

    *Triamcinolone acetonide
    is a steroid medicine
    known as a glucocorticoid.

    Principal Display Panel NDC 41167-5800-3 Multi-Symptom Nasal Allergy Spray Nasacort Allergy 24HR triamcinolone acetonide nasal spray 55 mcg per spray allergy symptom reliever (glucocorticoid)* 0.37 fl. oz. (10.8 ml) 60 Sprays *Triamcinolone acetonide is a steroid medicine known as a glucocorticoid.

  • Principal Display Panel

    Original Prescription Strength
    NDC 41167-5800-5
    Multi-Symptom
    Nasal Allergy Spray
    Nasacort
    Allergy 24HR
    triamcinolone acetonide nasal spray 55 mcg per spray
    allergy symptom reliever
    (glucocorticoid)*
    0.57 fl. oz. (16.9 ml) 120 Sprays

    *Triamcinolone acetonide
    is a steroid medicine
    known as a glucocorticoid.

    Principal Display Panel Original Prescription Strength NDC 41167-5800-5 Multi-Symptom Nasal Allergy Spray Nasacort Allergy 24HR triamcinolone acetonide nasal spray 55 mcg per spray allergy symptom reliever (glucocorticoid)* 0.57 fl. oz. (16.9 ml) 120 Sprays *Triamcinolone acetonide is a steroid medicine known as a glucocorticoid.

  • Principal Display Panel

    Nasacort Allergy 24HR
    Multi-Symptom
    Nasal Allergy Spray
    Insert

    Principal Display Panel Nasacort Allergy 24HR Multi-Symptom Nasal Allergy Spray Insert

  • INGREDIENTS AND APPEARANCE
    NASACORT ALLERGY 24HR 
    triamcinolone acetonide spray, metered
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-5800
    Route of AdministrationNASAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRIAMCINOLONE ACETONIDE (UNII: F446C597KA) (TRIAMCINOLONE ACETONIDE - UNII:F446C597KA) TRIAMCINOLONE ACETONIDE55 ug
    Inactive Ingredients
    Ingredient NameStrength
    CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    HYDROCHLORIC ACID (UNII: QTT17582CB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41167-5800-73 in 1 CARTON02/03/201407/31/2023
    1120 in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    2NDC:41167-5800-31 in 1 CARTON02/03/2014
    260 in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    3NDC:41167-5800-51 in 1 CARTON02/03/2014
    3120 in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    4NDC:41167-5800-22 in 1 CARTON02/03/2014
    4120 in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    5NDC:41167-5800-11 in 1 CARTON09/07/2017
    530 in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    6NDC:41167-5800-64 in 1 CARTON07/01/2021
    6120 in 1 BOTTLE, SPRAY; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    NDANDA02046802/03/2014
    Labeler - Chattem, Inc. (003336013)
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