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CounterAct Allergy

Medically reviewed by Drugs.com. Last updated on Feb 15, 2021.

Dosage form: tablet
Ingredients: LORATADINE 10mg
Labeler: Melaleuca, Inc.
NDC Code: 54473-166

CounterAct Allergy Content of Label

Active ingredient (in each tablet)
Loratadine 10 mg

Purpose
Antihistamine

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

COUNTERACT  ALLERGY
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54473-166
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE 
MAGNESIUM STEARATE 
POVIDONE 
STARCH, CORN 
Product Characteristics
Colorwhite (White colored) Scoreno score
ShapeOVAL (Oval shaped) Size8mm
FlavorImprint CodeL612
Contains    
Packaging
#Item CodePackage Description
1NDC:54473-166-303 BLISTER PACK in 1 CARTON
110 TABLET in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07520906/28/2008
Labeler - Melaleuca, Inc. (139760102)

 
Melaleuca, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.