LORATADINE ALLERGY RELIEF- loratadine tablet 
DISCOUNT DRUG MART

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Loratadine Allergy Relief

Active ingredient (in each tablet)

Loratadine USP, 10 mg

Purpose

Antihistamine

Uses

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 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

Other information

Inactive ingredients

corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch

Questions?

call 1-800-406-7984

DISTRIBUTED BY
DRUG MART-FOOD FAIR
MEDINA, OHIO 44256

PRINCIPAL DISPLAY PANEL - 10 mg Tablet Bottle Label

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FOOD FAIR

Non-Drowsy†

Allergy Relief

Loratadine
Tablets USP, 10 mg

Antihistamine
Indoor & Outdoor Allergies

RELIEF OF: Sneezing; Runny Nose
Itchy, Watery Eyes
Itchy Throat or Nose

24 Hour Allergy Relief

60 Tablets

†When taken as directed. See Drug Facts Panel.

Principal Display Panel - 10 mg Tablet Bottle Label
LORATADINE ALLERGY RELIEF 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53943-975
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
STARCH, CORN (UNII: O8232NY3SJ)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
Product Characteristics
Colorwhite (White to Off White) Scoreno score
ShapeROUNDSize6mm
FlavorImprint Code RX526
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53943-975-3030 in 1 BLISTER PACK; Type 0: Not a Combination Product11/01/2017
2NDC:53943-975-6060 in 1 BOTTLE; Type 0: Not a Combination Product11/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07613411/01/2017
Labeler - DISCOUNT DRUG MART (047741335)
Registrant - Ranbaxy Pharmaceuticals Inc. (937890044)
Establishment
NameAddressID/FEIBusiness Operations
Ohm Laboratories Inc.184769029manufacture(53943-975)

Revised: 9/2018
Document Id: 4ee4c604-4a18-4955-8b5e-b2eeff1cb7f8
Set id: 55d3ee36-116b-4ec6-b409-79d67a2b54ae
Version: 1
Effective Time: 20180914
 
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