Gencare-Allergy Relief
- Dosage form
- TABLET
- Labeler
- Pioneer Life Sciences, LLC
- Label updated
- 2026-06-22
- Retrieved
- 2026-09-07
- Active ingredients
- FEXOFENADINE HYDROCHLORIDE
Active ingredient (in each tablet)
Fexofenadine HCl 60 mg
Purpose
Antihistamine
Uses
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
■ runny nose
■ itchy, watery eyes
■ sneezing
■ itching of the nose or throat
Warnings
Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
Label information
Ask a doctor before use if you have kidney disease. Your doctor should determine if you need a different dose.
Label information
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)
Label information
Stop use and ask doctor if an allergic reaction to this product occurs. Seek medical help right away.
Label information
If pregnant or breast feeding, ask a health professional before use.
Label information
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
Directions
- Adults and children 12 years of age and over: Take one 60 mg tablet with water every 12 hours; do not take more than 2 tablets 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
Other Information
■ Store between 20°to 25°C (68°to 77°F)
■ Protect from excessive moisture
Inactive ingredients
Pregelatinized starch, corn starch, lactose monohydrate, colloidal silicon dioxide, croscarmellose sodium, anhydrous lactose, stearic acid, hypromellose, titanium dioxide, polyethylene glycol, yellow iron oxide, red iron oxide
Questions or comments?
Call +1 (732) 994-2808 or email [email protected]
NDC 72090-068-01 (100s Tablets in Bottle Pack)
[Image in the official label — see DailyMed source]
DailyMed Set ID: a8595b29-1ea3-44aa-b131-030f34f408fc · Version 1
NDC: 72090-068