Allegra Allergy

Allegra Allergy is an FDA-registered drug product whose active ingredient is FEXOFENADINE HYDROCHLORIDE. It is labelled by Navajo Manufacturing Company Inc. taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 67751-033, application NDA020872, label effective 20260422. It is one of 56 FDA drug label records sharing the active ingredient FEXOFENADINE HYDROCHLORIDE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing FEXOFENADINE HYDROCHLORIDE are most often described in connection with: temporarily relieves, symptoms due, hay fever, upper respiratory, allergies runny, nose sneezing, itchy watery, eyes itching. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses temporarily relieves these symptoms due to hay fever or upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat

Directions adults and children 12 years of age and over take one 180mg tablet with water once a day; do not take more than 1 tablet in 24 hours children under 12 years of age do not use adults 65 years of age and older ask a doctor consumers with kidney disease ask a doctor

Warnings Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Ask a doctor before use if you have kidney desease. Your doctor should determine ifyou need a different dose. When using this product do not take more than directed do not take at the same time as aluminum or magnesium antacids do not take with fruit juices (see Directions) Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. 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.

FDA lists 56 drug label records with FEXOFENADINE HYDROCHLORIDE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Allegra Allergy used for?
Uses temporarily relieves these symptoms due to hay fever or upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat

Who makes Allegra Allergy?
Navajo Manufacturing Company Inc. is the labeler of record for Allegra Allergy. 56 FDA label records share the active ingredient FEXOFENADINE HYDROCHLORIDE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Allegra Allergy come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Allegra Allergy prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing FEXOFENADINE HYDROCHLORIDE?
Yes. 56 FDA drug label records list FEXOFENADINE HYDROCHLORIDE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Allegra Allergy been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.