Label: CLARITIN REDITABS- loratadine tablet, orally disintegrating
- NDC Code(s): 11523-7202-1, 11523-7202-3
- Packager: Bayer HealthCare LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 10, 2023
If you are a healthcare professional or from the pharmaceutical industry please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each tablet)
- Purpose
- Uses
-
Warnings
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.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL - 10 Tablet Carton
NDC 11523-7202-3
Non-Drowsy*
Claritin ®
RediTabs ®
loratadine 5 mg/antihistamineIndoor & Outdoor
Allergies*When taken as directed. See Drug Facts Panel.
12
HourRelief of:
- Sneezing
- Runny Nose
- Itchy, Watery Eyes
-
Itchy Throat
or Nose
No Water Needed
Melts in Your Mouth10
ORALLY
DISINTEGRATING TABLETS -
INGREDIENTS AND APPEARANCE
CLARITIN REDITABS
loratadine tablet, orally disintegratingProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11523-7202 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 5 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 (flat faced beveled edge) Size 12mm Flavor MINT Imprint Code C5 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11523-7202-1 3 in 1 CARTON 12/12/2006 1 10 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:11523-7202-3 1 in 1 CARTON 12/12/2006 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 NDA021993 12/12/2006 Labeler - Bayer HealthCare LLC (112117283)