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Loratadine by Atlantic Biologicals Corps

Medically reviewed on August 16, 2018

Dosage form: solution
Ingredients: Loratadine 5mg in 5mL
Labeler: Atlantic Biologicals Corps
NDC Code: 17856-6234

Children's Loratadine Oral Solution

Active Ingredient: Loratadine 5 mg (in each 5 mL(teaspoonful)(TSP))

Purpose: Antihistamine

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

Warnings

ever had allergic reaction to this product or any of it's ingredients Do not use if you have

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

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

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

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

. In case of overdose, get medical help or contact a Poison Control Center right away. Keep out of reach of children

Directions
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

Other information
  • : sodium 1 mg Each teaspoonful contains
  • Safety Sealed. Do not use if imprinted seal around cap is broken or missing
  • Store between 20° to 25°C (68° to 77°F)

Inactive ingredients

Butylated hydroxylanisole, citric acid, glycerin, grape flavor, propylene glycol, purified water, sodium benzoate, sucralose.

Questions

1-800-616-2471

Distributed by: Major Pharmaceuticals 31778 Enterprise Drive, Livonia, MI 48150 USA



LORATADINE SOLUTION
LORATADINE  
loratadine solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17856-6234(NDC:0904-6234)
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Loratadine (Loratadine) Loratadine5 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
anhydrous citric acid 
butylated hydroxyanisole 
glycerin 
propylene glycol 
sodium benzoate 
sucralose 
water 
Product Characteristics
Color    Score    
ShapeSize
FlavorGRAPE (grape flavor) Imprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:17856-6234-25 mL in 1 CUP
2NDC:17856-6234-55 mL in 1 CUP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07742102/17/2011
Labeler - Atlantic Biologicals Corps (047437707)
Registrant - Atlantic Biologicals Corps (047437707)
Establishment
NameAddressID/FEIOperations
Atlantic Biologicals Corps047437707RELABEL(17856-6234), REPACK(17856-6234)

 
Atlantic Biologicals Corps

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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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