loratadine tablet, chewable

loratadine tablet, chewable
SPL v3
SPL
SPL Set ID 087ee83f-71aa-3d47-e063-6394a90aed4d
Route
oral
Published
Effective Date 2021-04-01
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
loratadine (5 mg)
Inactive Ingredients
aspartame anhydrous citric acid silicon dioxide magnesium stearate mannitol microcrystalline cellulose sodium starch glycolate type a potato stearic acid

Identifiers & Packaging

Pill Appearance
Imprint: LC5 Shape: round Color: white Size: 10 mm Score: 1
Marketing Status
anda active Since 2024-03-15

Purpose

Antihistamine

Description

Loratadine USP, 5 mg


Medication Information

Warnings

Do not useif you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you haveliver or kidney disease. Your doctor should determine if you need a different dose.

When using this productdo not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctorif an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or beast-feeding, ask a health professional before use.

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
Purpose

Antihistamine

Directions
  • chew or crush tablets completely before swallowing.

adults and children 6 years and over

chew 2 tablets daily; not more than 2 chewable tablets in 24 hours

children 2 to under 6 years of age

chew 1 tablet daily; not more than 1 chewable tablet in 24 hours

children under 2 years of age

ask a doctor

consumers with liver or kidney disease

ask a doctor

Other Information
  • phenylketonurics: contains phenylalanine 1.25 mg per tablet.
  • TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
  • store between 20° to 25°C (68° to 77°F).
Inactive Ingredients

aspartame, citric acid anhydrous, colloidal silicon dioxide, flavor, magnesium stearate, mannitol, microcrystalline cellulose, sodium starch glycolate, stearic acid

Description

Loratadine USP, 5 mg

Questions?

1800-632-6900

Keep Out of Reach of Children

In case of overdose, get medical help or contact a Poison Control Center right away (1800-222-1222).

Package/label Principal Display Panel

Active Ingredient (in Each Chewable Tablet)

Loratadine USP, 5 mg


Structured Label Content

Warnings

Do not useif you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you haveliver or kidney disease. Your doctor should determine if you need a different dose.

When using this productdo not take more than directed. Taking more than directed may cause drowsiness.

Stop use and ask a doctorif an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or beast-feeding, ask a health professional before use.

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
Purpose

Antihistamine

Directions
  • chew or crush tablets completely before swallowing.

adults and children 6 years and over

chew 2 tablets daily; not more than 2 chewable tablets in 24 hours

children 2 to under 6 years of age

chew 1 tablet daily; not more than 1 chewable tablet in 24 hours

children under 2 years of age

ask a doctor

consumers with liver or kidney disease

ask a doctor

Other Information (Other information)
  • phenylketonurics: contains phenylalanine 1.25 mg per tablet.
  • TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
  • store between 20° to 25°C (68° to 77°F).
Inactive Ingredients (Inactive ingredients)

aspartame, citric acid anhydrous, colloidal silicon dioxide, flavor, magnesium stearate, mannitol, microcrystalline cellulose, sodium starch glycolate, stearic acid

Questions?

1800-632-6900

Keep Out of Reach of Children

In case of overdose, get medical help or contact a Poison Control Center right away (1800-222-1222).

Package/label Principal Display Panel (Package/Label Principal Display Panel)

Active Ingredient (in Each Chewable Tablet) (Active ingredient (in each chewable tablet))

Loratadine USP, 5 mg


Advanced Ingredient Data


Raw Label Data

All Sections (JSON)