CLARITIN ALLERGY- loratadine solution 
Bayer HealthCare LLC.

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Claritin Liquid Cooling Honey UI 1613938

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:

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

Adults and children 6 years and over: 10 mL daily, do not take more than 10mL in 24 hours; children 2 to under 6 years of age: 5mL daily, do not take more than 5mL in 24 hours; children under 2 years of age: ask a doctor

Other Information

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

Questions or comments?

1-800-CLARITIN (1-800-252-7484)

Carton

CLARITIN  ALLERGY
loratadine solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-0101
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SORBITOL (UNII: 506T60A25R)  
MALTITOL (UNII: D65DG142WK)  
GLYCERIN (UNII: PDC6A3C0OX)  
PHOSPHORIC ACID (UNII: E4GA8884NN)  
SUCRALOSE (UNII: 96K6UQ3ZD4)  
WATER (UNII: 059QF0KO0R)  
SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Product Characteristics
Coloryellow (Clear, colorless to light yellow) Score    
ShapeSize
FlavorHONEYImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11523-0101-11 in 1 CARTON06/28/2024
130 mL in 1 BOTTLE; Type 0: Not a Combination Product
2NDC:11523-0101-21 in 1 CARTON06/28/2024
280 mL in 1 BOTTLE; Type 0: Not a Combination Product
3NDC:11523-0101-31 in 1 CARTON06/28/2024
3240 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02064105/22/2024
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 5/2024
Document Id: 19afd658-8c66-af44-e063-6394a90abada
Set id: 19afd658-8c67-af44-e063-6394a90abada
Version: 1
Effective Time: 20240530
 
Bayer HealthCare LLC.