Loratadine

Loratadine, USP 10 mg

Antihistamine

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

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

liver or kidney disease.Your doctor should determine if you need a different dose.

When using this product

do not take more than directed. Taking more than directed may cause drowsiness.

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.

adults and children 6 years and over	1 tablet daily; not more than 1 tablet in 24 hours
children under 6 years of age	ask a doctor
consumers with liver or kidney disease	ask a doctor

• •Safety sealed: do not use if the imprinted bottle seal is open or torn (for bottle only).
• •Safety sealed: do not use if open or torn (for blister package only).

보관·기타 정보

• •Store at 20° to 25°C (68° to 77°F) (see USP Controlled Room Temperature).

Lactose monohydrate, magnesium stearate, microcrystalline cellulose and sodium starch glycolate.

1-800-206-7821

Label information

© 2005 NorthStar Healthcare Holdings     I10-2015M

Manufactured for: Northstar Rx LLC

Memphis, TN 38141.

Manufactured by: Sandoz Inc.

Princeton, NJ 08540.

Product: 50090-3620

NDC: 50090-3620-0 10 TABLET in a BOTTLE

NDC: 50090-3620-3 15 TABLET in a BOTTLE, PLASTIC

NDC: 50090-3620-4 30 TABLET in a BOTTLE, PLASTIC

NDC: 50090-3620-5 90 TABLET in a BOTTLE, PLASTIC

NDC: 50090-3620-1 20 TABLET in a BOTTLE, PLASTIC

NDC: 50090-3620-6 7 TABLET in a BOTTLE, PLASTIC

[Image in the official label — see DailyMed source]