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Loratadine

Dosage form
TABLET
Labeler
AvPAK
Label updated
2026-05-21
Retrieved
2026-09-07
Active ingredients
LORATADINE
View original label and images on DailyMed ↗
ACTIVE INGREDIENT(S)

Active ingredient (in each tablet)          
Loratadine USP, 10 mg


PURPOSE

Antihistamine

USE(S)

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 DOCTOR IF

an allergic reaction to this product occurs. Seek medical help right away.

PREGNANCY/BREASTFEEDING

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

Bottles:    

  • 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)

Blisters packs:

  • safety sealed: do not use if the individual blister unit imprinted with loratadine is open or torn
  • store between 20° to 25°C (68° to 77°F)
  • protect from excessive moisture
INACTIVE INGREDIENTS

corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch

QUESTIONS OR COMMENTS?

Call 1-855-361-3993

Manufactured for:

AvKARE

Pulaski, TN 38478

www.avkare.com

PRINCIPAL DISPLAY PANEL

[Image in the official label — see DailyMed source]

DailyMed Set ID: 52581dd2-9597-35cb-e063-6294a90a36c7 · Version 1
NDC: 50268-777