CLARITIN - loratadine tablet 
Schering-Plough HealthCare Products, Inc.

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Non-Drowsy*
Claritin®
loratadine tablets 10 mg/antihistamine

Drug Facts

Active ingredient (in each tablet)

Loratadine 10 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.

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.

Directions

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

Other information

• Tamper-evident: do not use if foil seal under cap, printed with "SEALED for YOUR PROTECTION" is missing, open or broken
• store between 20° to 25°C (68° to 77°F)

Inactive ingredients

corn starch, lactose monohydrate, magnesium stearate

Questions or comments?

1-800-CLARITIN (1-800-252-7484) or www.claritin.com

PRINCIPAL DISPLAY PANEL - 45 Tablet Carton

Original Prescription
Strength

NDC 11523-7237-1

Non-Drowsy*
Claritin®
loratadine tablets 10 mg/antihistamine

24
Hour

Relief of:

• Sneezing
• Runny Nose
• Itchy, Watery Eyes
• Itchy Throat or Nose

Indoor & Outdoor
Allergies

*When taken as directed.
See Drug Facts Panel.

45 TABLETS

CLARITIN  loratadine   tablet

Product Information Product Type HUMAN OTC DRUG NDC Product Code (Source) 11523-7237 Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Loratadine (Loratadine) Loratadine 10 mg

Inactive Ingredients Ingredient Name Strength starch, corn   lactose monohydrate   magnesium stearate

Product Characteristics Color WHITE Score no score Shape ROUND Size 6mm Flavor Imprint Code 458;10 Contains

Packaging # NDC Package Description Multilevel Packaging 1 11523-7237-1 1 BOTTLE In 1 CARTON contains a BOTTLE 1 45 TABLET In 1 BOTTLE This package is contained within the CARTON (11523-7237-1) 2 11523-7237-5 1 BOTTLE In 1 PACKAGE contains a BOTTLE 2 90 TABLET In 1 BOTTLE This package is contained within the PACKAGE (11523-7237-5)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
NDA	NDA019658	04/12/1993

Labeler - Schering-Plough HealthCare Products, Inc. (039137567)

Revised: 12/2010Schering-Plough HealthCare Products, Inc.