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Loratadine

Dosage form
TABLET
Labeler
Preferred Pharmaceuticals Inc.
Label updated
2026-05-28
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 noseitchy, watery eyessneezingitching 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

Repackaged By: Preferred Pharmaceuticals Inc.

QUESTIONS OR COMMENTS?

Call 1-888-588-1418

PRINCIPAL DISPLAY PANEL

Loratadine-tablets-USP-10mg-

 

[Image in the official label — see DailyMed source]

DailyMed Set ID: d778c4d2-184a-4dc8-9351-66d81d0618f2 · Version 3
NDC: 68788-8605