CLARITIN REDITABS- loratadine tablet, orally disintegrating 
Bayer Healthcare LLC

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Claritin ®

RediTabs ®

Drug Facts

Active ingredient (in each tablet)

Loratadine 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

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

anhydrous citric acid, gelatin, mannitol, mint flavor

Questions or comments?

1-800-CLARITIN (1-800-252-7484) or www.claritin.com

Distributed by MSD Consumer Care, Inc.,
PO Box 377, Memphis, TN 38151 USA,
a subsidiary of Merck & Co., Inc., Whitehouse Station, NJ USA.

PRINCIPAL DISPLAY PANEL - 10 Tablet Carton

Original Prescription Strength
NDC 11523-7157-2

Non-Drowsy*
Claritin
®
RediTabs®
loratadine 10 mg/antihistamine

Indoor & Outdoor
Allergies

*When taken as directed. See Drug Facts Panel.

24
Hour

Relief of:

No Water Needed
Melts in Your Mouth

10
ORALLY
DISINTEGRATING TABLETS

PRINCIPAL DISPLAY PANEL - 10 Tablet Carton

PRINCIPAL DISPLAY PANEL - 60 Tablet Twin Pack Carton

TWIN PACK

Two 30ct Cartons
60 RediTabs
®

Original Prescription Strength

NDC 11523-4329-1

Non-Drowsy*
Claritin
®
RediTabs®
loratadine 10 mg/antihistamine

Indoor & Outdoor
Allergies

*When taken as directed. See Drug Facts Panel.

24
Hour

Relief of:

No Water Needed
Melts in Your Mouth

60
ORALLY
DISINTEGRATING TABLETS

PRINCIPAL DISPLAY PANEL - 60 Tablet Twin Pack Carton
CLARITIN  REDITABS
loratadine tablet, orally disintegrating
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:11523-7157
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 10 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GELATIN (UNII: 2G86QN327L)  
MANNITOL (UNII: 3OWL53L36A)  
Product Characteristics
Color white Score no score
Shape ROUND Size 12mm
Flavor MINT Imprint Code C10
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11523-7157-2 1 in 1 CARTON 11/27/2002
1 10 in 1 BLISTER PACK; Type 0: Not a Combination Product
2 NDC:11523-7157-3 3 in 1 CARTON 11/27/2002
2 10 in 1 BLISTER PACK; Type 0: Not a Combination Product
3 NDC:11523-7157-4 2 in 1 CARTON 11/27/2002
3 10 in 1 BLISTER PACK; Type 0: Not a Combination Product
4 NDC:11523-7157-7 4 in 1 CARTON 11/27/2002
4 10 in 1 BLISTER PACK; Type 0: Not a Combination Product
5 NDC:11523-7157-8 5 in 1 CARTON 11/27/2002
5 10 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020704 11/27/2002
CLARITIN  REDITABS
loratadine tablet, orally disintegrating
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:11523-4329
Route of Administration ORAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 10 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
GELATIN (UNII: 2G86QN327L)  
MANNITOL (UNII: 3OWL53L36A)  
Product Characteristics
Color white Score no score
Shape ROUND Size 12mm
Flavor MINT Imprint Code C10
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:11523-4329-1 2 in 1 PACKAGE, COMBINATION 11/27/2002
1 3 in 1 CARTON
1 10 in 1 BLISTER PACK; Type 0: Not a Combination Product
2 NDC:11523-4329-2 6 in 1 CARTON 11/27/2002
2 10 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA020704 11/27/2002
Labeler - Bayer Healthcare LLC (968091715)

Revised: 6/2016
Document Id: 3454e6c8-e526-13fd-e054-00144ff88e88
Set id: b681ea25-d00b-4c8a-8054-cc6f983ce337
Version: 5
Effective Time: 20160602
 
Bayer Healthcare LLC