ALLERGY RELIEF NON DROWSY - loratadine tablet 
Select Corporation

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Drug Facts

Active Ingredients

Loratadine USP 10 mg

Antihistamine

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

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.

Inactive
ingredients: corn starch, lactose monohydrate,
magnesium stearate, pregelatinized starch

MM1

Allergy Non Drowsy packet

ALLERGY RELIEF NON DROWSY 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52904-430
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
MAGNESIUM STEARATE (UNII: 70097M6I30)  
LACTOSE (UNII: J2B2A4N98G)  
STARCH, CORN (UNII: O8232NY3SJ)  
Product Characteristics
Colorwhite (snow white) Scoreno score
ShapeROUND (RX526) Size6mm
FlavorImprint Code RX526
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52904-430-011 in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07715310/15/2012
Labeler - Select Corporation (053805599)
Registrant - Select Corporation (053805599)

Revised: 10/2012
Document Id: 467fa578-bb0b-48dd-b5e2-36e5e9829c96
Set id: f14b202e-56bd-4477-84c9-2d99ac38c111
Version: 1
Effective Time: 20121015
 
Select Corporation