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Children Claritin Allergy by Famar Montreal Inc

Medically reviewed on Apr 27, 2017

Dosage form: solution
Ingredients: LORATADINE 5mg in 5mL
Labeler: Famar Montreal Inc
NDC Code: 69213-4360

Children's Claritin Allergy (Grape Flavor)

Drug Facts

Active ingredient (in each 5 mL teaspoonful)

Loratadine 5 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • runny nose
  • sneezing
  • itchy, watery eyes
  • 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

Use only with enclosed dosing cup

  • adults and children 6 years and over: 2 teaspoonfuls (tsp) daily; do not take more than 2 teaspoonfuls (tsp) in 24 hours
  • children 2 to under 6 years of age: 1 teaspoonful (tsp) daily; do not take more than 1 teaspoonful (tsp) in 24 hours
  • children under 2 years of age: ask a doctor
  • consumers with liver or kidney disease: ask a doctor

  • each teaspoonful contains: sodium 6 mg
  • do not use if tape imprinted with “SEALED FOR YOUR PROTECTION” on top and bottom flaps of carton is not intact.
  • store between 20° and 25°C (68° and 77°F)

edetate disodium, flavor, glycerin, maltitol, monobasic sodium phosphate, phosphoric acid, propylene glycol, purified water, sodium benzoate, sorbitol, sucralose

Questions or comments?

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

CHILDREN CLARITIN  ALLERGY
loratadine solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69213-4360
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BENZOATE 
SORBITOL 
EDETATE DISODIUM 
MALTITOL 
GLYCERIN 
PHOSPHORIC ACID 
SUCRALOSE 
WATER 
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPEImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:69213-4360-51 BOTTLE in 1 CARTON
1240 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02064105/26/2015
Labeler - Famar Montreal Inc (203565379)

 
Famar Montreal Inc

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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