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Budesonide

s Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • itchy nose • sneezing.

Sold without prescription in some countries Nasal Safety alerts on record

How to use Budesonide

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

S Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • itchy nose • sneezing

How to take it and how often
  • Read insert (inside package) on how to: get a new bottle ready (primed) before first use prime bottle again if not used for two days 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 6 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 under 6 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 two weeks, stop using and talk to a doctor do not use for the common cold
  • Shake well before each use
While you are taking it
  • 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 two weeks 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
Talk to a doctor first if

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

Warnings

Do not use in children under 6 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 two weeks of daily use to feel the most symptom relief. …

Possible side effects

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

Pregnancy and breastfeeding

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

How to store it

Keep out of reach of children.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2026-02-27.

Brands around the world

Products with Budesonide as the active ingredient. Names differ between countries.

Registered products

United States (FDA)

Budesonide MicronizedBUDESONIDE 3.4 kg/3.4kg · Powder · AstraZeneca AB
NDC 17228-1991Label
Budesonide InhalationBUDESONIDE .5 mg/2mL · Suspension · Lupin Pharmaceuticals, Inc.
NDC 68180-984Label
Budesonide Inhalation Suspension Inhalation SuspensionBUDESONIDE .25 mg/2mL · Inhalant · Cipla USA Inc.
NDC 69097-318Label
Budesonide Inhalation Suspension Inhalation SuspensionBUDESONIDE .5 mg/2mL · Inhalant · Cipla USA Inc.
NDC 69097-319Label
Budesonide Inhalation Suspension Inhalation SuspensionBUDESONIDE 1 mg/2mL · Inhalant · Cipla USA Inc.
NDC 69097-321Label

Nigeria (NAFDAC)

NAFDACFortide DPI_ A4-101656NAFDACPulmicort Nebulising Suspension A4-6468NAFDACPulmicort Nebulising Suspension A4-6469NAFDACSymbicort 80/4.5 mcg Turbuhaler A4-7006NAFDACSymbicort 160/4.5 mcg Turbuhaler A4-7007NAFDACBudesone-100 Inhaler## (check composition) C4-1503NAFDACBudesone-200 Inhaler## (check composition) C4-1504NAFDACFortide Inhaler 200 mcg + 6 mcg## (strength format) B4-9410

Other countries: check your pack's registration number and we point you to your regulator.

Safety alerts and recalls

Budesonide Inhalation Suspension, 1mg/2mL, 30 x 2 mL Sterile Single-Dose Ampules (5 Single-Dose Ampules per pouch, 6 pouches per carton, Distributed by: Sun Pharmaceutical IndustriU.S. FDA Class II
29 May 2026 · SUN PHARMACEUTICAL INDUSTRIES INC · OngoingPresence of Foreign Substance:This recall has been initiated in response to a product quality complaint reported for black/brown specs and particles within the ampoule solution
Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per pouch, RX Only, Manufactured by: Cipla Ltd. Indore SEZ, Pithampur, India. Manufactured for:U.S. FDA Class II
30 Jun 2025 · Cipla USA, Inc. · OngoingLack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule.
Airsupra (albuterol and budesonide) inhalation aerosol, 90 mcg/80 mcg per inhalation, packaged in a) 120-inhalation canister (NDC 0310-9080-12) b) 28-inhalation canister (NDC 0310-U.S. FDA Class II
14 May 2025 · AsttraZeneca Pharmaceuticals LP · OngoingDefective delivery system
Budesonide, USP (Micronized), 500 mg, White to off-white odorless, crystalline powder, Medisca Inc., Plattsburgh, NY, 12901, USA, NDC: 38779-3097-00.U.S. FDA Class II
26 Jun 2024 · Medisca Inc. · CompletedCGMP Deviations and Presence of Particulate Matter: Glass

A recall usually affects certain batches only. Compare the lot number on your pack.

Check your pack of Budesonide

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

Questions about Budesonide

What is Budesonide used for?

s Temporarily relieves these symptoms of hay fever or other upper respiratory allergies: • nasal congestion • runny nose • itchy nose • sneezing (From the official U.S. FDA label.)

How do I take Budesonide?

Follow your prescription or the leaflet in your pack. The official label says: Read insert (inside package) on how to: get a new bottle ready (primed) before first use prime bottle again if not used for two days 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 spra…

Do I need a prescription for Budesonide?

In many countries Budesonide is sold without a prescription in some strengths. Rules differ by country, so ask a pharmacist.

What brands contain Budesonide?

Budesonide is sold under names such as Uceris, Entocort, Pulmicort, Rhinocort, Ortikos, Breztri, Tarpeyo, Breyna. Brand names differ between countries.

How can I check that my Budesonide is genuine?

Scan the registration number on your pack with PillVera (NAFDAC number in Nigeria, NDC in the United States, DIN in Canada), check the expiry date and buy only from licensed pharmacies.