Allegra Allergy 24 hour
Allegra Allergy 24 hour is an FDA drug label for the active ingredient FEXOFENADINE HYDROCHLORIDE manufactured by Select Consumer Group administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260601.
- Generic name
- FEXOFENADINE HYDROCHLORIDE
- Manufacturer
- Select Consumer Group
- Product type
- HUMAN OTC DRUG
- Route
- ORAL
- Dosage form
- N/A
- NDC
- 85237-1920
- Application
- M012
- Label effective
- 20260601
About this product
Allegra Allergy 24 hour is an FDA-registered drug product whose active ingredient is FEXOFENADINE HYDROCHLORIDE. It is labelled by Select Consumer Group taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 85237-1920, application M012, label effective 20260601. 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.
Active ingredients
Indications & Usage
Antihistamine
Dosage & Administration
adults and children 12 years of age and over take one 180 mg 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 disease. Your doctor should determine if you 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.
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View labelHow products containing FEXOFENADINE HYDROCHLORIDE compare
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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Aurohealth LLC | 3 |
| — | — | HEB | 2 |
| — | — | NUVICARE LLC | 2 |
| — | — | YYBA Corp | 2 |
| — | — | 7-eleven | 1 |
Frequently asked questions
What is Allegra Allergy 24 hour used for?
Antihistamine
Who makes Allegra Allergy 24 hour?
Select Consumer Group is the labeler of record for Allegra Allergy 24 hour. 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 24 hour 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 24 hour 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 24 hour 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.