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Allergy Relief

제형
TABLET
업체
NUVICARE LLC
원문 갱신
2026-05-21
가져온 날
2026-09-07
유효 성분
FEXOFENADINE HYDROCHLORIDE
DailyMed 원문·등록 이미지 확인 ↗
Drug FactsDrug Facts

유효 성분Active ingredient (in each tablet)

Fexofenadine HCl 180 mg

성분·작용Purpose

Antihistamine

효능·용도Uses

Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

■ runny nose

■ sneezing

■ itchy, watery eyes

■ itching of the nose or throat

주의사항Warnings

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 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.

기타 원문Label 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.

복용법·사용법Directions
 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

Other InformationOther Information

■ Store between 20°to 25°C (68°to 77°F)

■ Protect from excessive moisture

첨가제Inactive ingredients

Microcrystalline cellulose, pregelatinized starch, croscarmellose sodium, colloidal silicon dioxide, magnesium stearte, hypromellose, lactose monohydrate, polyethylene glycol 6000, titanium dioxide, yellow iron oxide, red iron oxide, black iron oxide

제조사 문의Questions or comments?

Call 1 (718) 337-8733 or visit: [email protected]

포장 표시포장 표시

[Image in the official label — see DailyMed source]

DailyMed Set ID: 895de6e9-c5b6-42fe-b450-f5d8331ce2e3 · 버전 1
NDC: 84324-040