CAREALL ALLERGY RELIEF- loratadine tablet

CAREALL Allergy Relief by

Drug Labeling and Warnings

CAREALL Allergy Relief by is a Otc medication manufactured, distributed, or labeled by New World Imports. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Loratadine 10mg

PURPOSE

Antihistamine

KEEP OUT OF REACH OF CHILDREN

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

INDICATIONS & USAGE

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

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.

DOSAGE & ADMINISTRATION

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

INACTIVE INGREDIENT

lactose monohydrate, magnesium stearate, pregelatinized starch, sodium starch glycolate.  

OTHER SAFETY INFORMATION

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CAREALL ALLERGY RELIEF 
loratadine tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51824-103
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN)	LORATADINE	10 mg

Inactive Ingredients
Ingredient Name	Strength
MAGNESIUM STEARATE (UNII: 70097M6I30)
SODIUM STARCH GLYCOLATE TYPE A (UNII: H8AV0SQX4D)
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
STARCH, CORN (UNII: O8232NY3SJ)

Product Characteristics
Color	white (White to off white)	Score	no score
Shape	ROUND	Size	6mm
Flavor		Imprint Code	G;10
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51824-103-30	30 in 1 BOTTLE; Type 0: Not a Combination Product	12/07/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA210722	12/07/2023

Labeler - New World Imports (075372276)

Registrant - New World Imports (075372276)