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Claritin Reditabs by Bayer Healthcare LLC

Medically reviewed on June 4, 2018

Dosage form: tablet, orally disintegrating
Ingredients: LORATADINE 10mg
Labeler: Bayer Healthcare LLC
NDC Code: 11523-7157

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:

  • runny nose
  • itchy, watery eyes
  • sneezing
  • 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. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions
  • place 1 tablet on tongue; tablet disintegrates, with or without water
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
  • safety sealed: do not use if the individual blister unit imprinted with Claritin® RediTabs® is open or torn
  • store between 20° to 25°C (68° to 77°F)
  • use tablet immediately after opening individual blister
  • complies with USP Procedure 2 for Assay and Organic Impurities and Test 2 for Disintegration

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:

  • Sneezing
  • Runny Nose
  • Itchy, Watery Eyes
  • Itchy Throat
    or Nose

No Water Needed
Melts in Your Mouth

10
ORALLY
DISINTEGRATING TABLETS

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:

  • Sneezing
  • Runny Nose
  • Itchy, Watery Eyes
  • Itchy Throat
    or Nose

No Water Needed
Melts in Your Mouth

60
ORALLY
DISINTEGRATING TABLETS

CLARITIN  REDITABS
loratadine tablet, orally disintegrating
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-7157
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID 
GELATIN 
MANNITOL 
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize12mm
FlavorMINTImprint CodeC10
Contains    
Packaging
#Item CodePackage Description
1NDC:11523-7157-21 BLISTER PACK in 1 CARTON
110 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
2NDC:11523-7157-33 BLISTER PACK in 1 CARTON
210 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
3NDC:11523-7157-42 BLISTER PACK in 1 CARTON
310 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
4NDC:11523-7157-74 BLISTER PACK in 1 CARTON
410 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
5NDC:11523-7157-85 BLISTER PACK in 1 CARTON
510 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02070411/27/2002
CLARITIN  REDITABS
loratadine tablet, orally disintegrating
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-4329
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LORATADINE (LORATADINE) LORATADINE10 mg
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID 
GELATIN 
MANNITOL 
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize12mm
FlavorMINTImprint CodeC10
Contains    
Packaging
#Item CodePackage Description
1NDC:11523-4329-12 CARTON in 1 PACKAGE, COMBINATION
13 BLISTER PACK in 1 CARTON
110 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
2NDC:11523-4329-26 BLISTER PACK in 1 CARTON
210 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02070411/27/2002
Labeler - Bayer Healthcare LLC (968091715)

 
Bayer Healthcare LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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