rexall allergy relief description, usages, side effects, indications, overdosage, supplying and lots more!

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rexall allergy relief

Dolgencorp, LLC

Dolgencorp, LLC Allergy Relief Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active ingredient (in each tablet)

Loratadine 10 mg

Purpose

Antihistamine

rexall allergy relief 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

adults and children 6 years and over 1 tablet daily; not 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

rexall allergy relief Other information

  • do not use if printed foil under cap is broken or missing
  • store at 20°-25°C (68°-77°F)

Inactive ingredients

lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Principal Display Panel

Non-Drowsy*

24 Hour

Actual Size

Allergy Relief

Loratadine Tablets, 10 mg/Antihistamine

Gluten Free

Relief of

Sneezing

Itchy, watery eyes

Runny nose

Itchy throat or nose

Original Prescription Strength

Indoor & outdoor allergies

*When taken as directed.

See Drug Facts Panel.

rexall allergy relief
Allergy Relief Carton Image 1 Allergy Relief Carton Image 2

rexall allergy relief

Loratadine TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55910-612
Route of Administration ORAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
LORATADINE loratadine 10 mg

Inactive Ingredients

Ingredient Name Strength
lactose monohydrate
MAGNESIUM STEARATE
povidone

Product Characteristics

Color Size Imprint Code Shape
WHITE 8 mm L612 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 30 in 1 BOTTLE
2 NDC:55910-612-65 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA076301 2010-08-22


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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