LORATADINE ALLERGY RELIEF- loratadine tablet 
OHM LABORATORIES INC.

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Loratadine Allergy Relief

Drug Facts

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 (1-800-222-1222).

Directions

adults and children 6 years and over1 tablet daily; not more than 1 tablet in 24 hours
children under 6 years of ageask a doctor
consumers with liver or kidney diseaseask a doctor

Other Information

Inactive ingredients

corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch

Questions?

call 1-800-406-7984

Distributed by:
Ohm Laboratories Inc.
New Brunswick, NJ 08901

PRINCIPAL DISPLAY PANEL - 10 mg Tablet Blister Pack Carton

Compare To
the active ingredient of
Claritin®

ohm®

NDC 51660-526-11

NON-DROWSY*
24 Hour
Allergy Relief

Original Prescription Strength
Allergy Relief
Loratadine Tablets, USP 10 mg
Antihistamine
Indoor & Outdoor Allergies

Relief of:

Sneezing
Runny Nose
Itchy, Watery Eyes
Itchy Throat or Nose

10 Tablets

* When taken as directed. See Drug Facts Panel.

PRINCIPAL DISPLAY PANEL - 10 mg Tablet Blister Pack Carton
LORATADINE ALLERGY RELIEF 
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51660-526
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:51660-526-01100 in 1 BOTTLE; Type 0: Not a Combination Product11/01/2017
2NDC:51660-526-05500 in 1 BOTTLE; Type 0: Not a Combination Product11/01/2017
3NDC:51660-526-53300 in 1 BOTTLE; Type 0: Not a Combination Product11/01/2017
4NDC:51660-526-3030 in 1 BOTTLE; Type 0: Not a Combination Product02/01/2019
5NDC:51660-526-3130 in 1 BLISTER PACK; Type 0: Not a Combination Product11/01/2017
6NDC:51660-526-1110 in 1 BLISTER PACK; Type 0: Not a Combination Product11/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07613411/01/2017
Labeler - OHM LABORATORIES INC. (184769029)
Establishment
NameAddressID/FEIBusiness Operations
Ohm Laboratories Inc.184769029MANUFACTURE(51660-526)

Revised: 12/2023
Document Id: ab379305-5823-49e9-89ca-641c1d37a6f3
Set id: c35f2cc1-f76d-4824-b0a5-747bca0c3b85
Version: 10
Effective Time: 20231208
 
OHM LABORATORIES INC.