Loratadine 10mg

Active ingredient (in each tablet)
Loratadine USP, 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 (1-800-222-1222). 

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

• For Bottle pack: Tamper-evident: do not use this product if the imprinted foil seal over the mouth of the bottle is cut, torn, broken or missing.
• For Blister pack: Tamper-evident: do not use if the individual blister unit is open or torn
• store between 20º to 25º C (68º to 77º F)
• FDA approved dissolution test specifications differ from USP

Inactive ingredients colloidal silicon dioxide, lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate

Questions or comments? Call 1-877-376-4271 (weekdays 9 AM to 5 PM)

Manufactured for:
Time-Cap Labs, Inc. 
7 Michael Avenue, 
Farmingdale, 
NY 11735

Manufactured by: 
Marksans Pharma Ltd.
Plot No. L-82, L-83
Verna Indl. Estate
Verna, Goa-403722 

Made in India

NDC: 25000-092-81
Loratadine Tablets USP, 10 mg
14's count Carton

[Image in the official label — see DailyMed source]

NDC: 25000-092-03
Loratadine Tablets USP, 10 mg
30's count Carton

[Image in the official label — see DailyMed source]

NDC: 25000-092-03
Loratadine Tablets USP, 10 mg
30's count Label

[Image in the official label — see DailyMed source]

NDC: 25000-092-79
Loratadine Tablets USP, 10 mg
150's count Carton

[Image in the official label — see DailyMed source]

NDC: 25000-092-79
Loratadine Tablets USP, 10 mg
150's count Label

[Image in the official label — see DailyMed source]

NDC: 25000-092-80
Loratadine Tablets USP, 10 mg
365's count Label

[Image in the official label — see DailyMed source]