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CounterAct

Melaleuca, Inc.

CounterAct Allergy Content of Label




FULL PRESCRIBING INFORMATION

Active ingredient

Active ingredient (in each tablet)
Loratadine 10 mg

Purpose

Purpose
Antihistamine

Uses

Use  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 processional 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








Other information

  • store at 20°-25°C (68°-77°F)
  • protect from excessive moisture
  • do not use if blister unit is broken or torn

Inactive ingredients  lactose monohydrate, magnesium stearate, povidone, pregelatinized starch

Questions or comments? 1-800-282-3000

CounterActCounterAct

CounterAct

Loratadine TABLET

Product Information

Product Type Human otc drug label Item Code (Source) NDC:54473-166
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
STARCH, CORN

Product Characteristics

Color Size Imprint Code Shape
white (White colored) 8 mm L612 OVAL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 10 in 1 BLISTER PACK
2 NDC:54473-166-30 3 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA075209 2008-06-28


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