CAREALL LORATADINE- loratadine tablet 
New World Imports

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Drug Facts

Loratadine 10mg

Antihistamine

In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222)

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

runny nose, itchy, watery eys, sneezing, itching 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 a doctor if an allergic reaction to this product occurs.  Seek medical help right away.

Adult and children over 6 years old: 1 tablets daily: no 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

lactose monohydrate, magnesium stearate, sodium starch glycolate.  May contain: microcrystalline cellulose, pregelatinized starch

Store between 20-25 degrees celcius (68-77 degrees farhenheit).

Protect from excessive moisture

Do not use if imprinted seal under bottle cap is broken or missing

You may report side effects 1-888-952-0050

Loratadine
CAREALL LORATADINE 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51824-075
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
MAGNESIUM STEARATE (UNII: 70097M6I30)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
STARCH, CORN (UNII: O8232NY3SJ)  
Product Characteristics
Colorwhite (White to off white) Scoreno score
ShapeROUNDSize6mm
FlavorImprint Code GG296;G;10
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51824-075-0130 in 1 BOTTLE; Type 0: Not a Combination Product03/02/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21072203/02/2020
Labeler - New World Imports (075372276)
Registrant - New World Imports (075372276)

Revised: 12/2023
Document Id: 49dda466-3496-49ec-a374-6182b5353b52
Set id: 4d952d2f-7766-4e64-8462-3fdff144546a
Version: 3
Effective Time: 20231207
 
New World Imports