Label: REXALL ALLERGY RELIEF NON DROWSY- loratadine tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 55910-612-65 - Packager: Dolgencorp, LLC
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated October 13, 2022
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- Official Label (Printer Friendly)
- Active ingredient (in each tablet)
- Purpose
- Uses
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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?
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Principal Display Panel
Since 1903 Rexall®
NON-DROWSY*
24 HOUR
Actual Size
Allergy Relief
Loratadine Tablets, 10 mg / Antihistamine
GLUTEN FREE
24 Hour relief of
• Sneezing
• Runny nose
• Itchy, watery eyes
• Itchy throat or nose
30 Tablets
Original Prescription Strength
*When taken as directed. See Drug Facts Panel.
Indoor & outdoor allergies
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INGREDIENTS AND APPEARANCE
REXALL ALLERGY RELIEF NON DROWSY
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-612 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 LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) Product Characteristics Color WHITE Score no score Shape OVAL Size 8mm Flavor Imprint Code L612 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-612-65 1 in 1 CARTON 08/22/2010 1 30 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076301 08/22/2010 Labeler - Dolgencorp, LLC (068331990)