COUNTERACT ALLERGY- loratadine tablet 
Melaleuca, Inc.

----------

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:

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

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

Questions or comments? 1-800-282-3000

Counteract Allergy LabelCounteract Allergy Box

COUNTERACT  ALLERGY
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54473-166
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
POVIDONE (UNII: FZ989GH94E)  
STARCH, CORN (UNII: O8232NY3SJ)  
Product Characteristics
Colorwhite (White colored) Scoreno score
ShapeOVAL (Oval shaped) Size8mm
FlavorImprint Code L612
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54473-166-313 in 1 BOX08/19/2023
110 in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07520908/19/2023
Labeler - Melaleuca, Inc. (139760102)

Revised: 8/2023
Document Id: 0338b445-8b01-bdf2-e063-6394a90a925d
Set id: 6b5d43ad-a709-4e0b-b91c-36ea0afe7221
Version: 3
Effective Time: 20230818
 
Melaleuca, Inc.