ALLERGY RELIEF NON DROWSY- loratadine tablet 
St Mary's Medical Park Pharmacy

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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 (1-800-222-1222) right away.

Directions

adults and children 6 years and over1 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, microcrystalline cellulose, sodium starch glycolate

Questions or comments?

Call 1-888-588-1418 Monday-Friday 9AM-5PM EST

Principal Display Panel

†Compare to the active ingredient in Claritin® 24 Hour

Non-drowsy*

Allergy Relief

Loratadine Tablets, USP 10 mg / Antihistamine

Indoor & outdoor  allergies

24 Hour Relief of:

Tablets

Gluten-Free

* When taken as directed. See Drug Facts panel.

†This product is not manufactured or distributed by Bayer Healthcare LLC, distributor of Claritin® 24 Hour

TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAPS IS BROKEN OR MISSING.

Distributed by:

Camber Consumer Care Inc., Piscataway, NJ 08854, USA

loratadine

ALLERGY RELIEF  NON DROWSY
loratadine tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60760-569(NDC:69230-317)
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)  
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B)  
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize6mm
FlavorImprint Code 439
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:60760-569-00100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA07520912/27/2019
Labeler - St Mary's Medical Park Pharmacy (063050751)
Establishment
NameAddressID/FEIBusiness Operations
St Mary's Medical Park Pharmacy063050751relabel(60760-569) , repack(60760-569)

Revised: 5/2022
Document Id: de5f9641-49c4-490a-e053-2a95a90af219
Set id: de5fa19f-25d9-ba81-e053-2a95a90af82f
Version: 3
Effective Time: 20220505
 
St Mary's Medical Park Pharmacy