Label: ALLERGY RELIEF- loratadine tablet
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NDC Code(s):
11822-0612-1,
11822-0612-2,
11822-0612-3,
11822-0612-4, view more11822-0612-5, 11822-0612-6, 11822-0612-7, 11822-0612-8, 11822-0612-9
- Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated June 14, 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)
- 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
FREE FROM
GLUTEN FREE
24 HOUR
Compare to the active ingredient of Claritin® Tablets
ORIGINAL PRESCRIPTION STRENGTH
ALLERGY RELIEF
LORATADINE TABLETS, 10 mg
ANTIHISTAMINE
NON-DROWSY*
INDOOR & OUTDOOR ALLERGIES
24 HOUR RELIEF OF
Sneezing • Runny nose
Itchy, watery eyes
Itchy throat or nose
ACTUAL SIZE
*WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.
30 TABLETS
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0612 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:11822-0612-2 1 in 1 CARTON 10/21/2004 1 10 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:11822-0612-1 3 in 1 CARTON 11/18/2004 2 10 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:11822-0612-3 1 in 1 CARTON 07/08/2005 3 60 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:11822-0612-4 1 in 1 CARTON 04/15/2005 4 120 in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:11822-0612-5 1 in 1 CARTON 01/23/2014 5 45 in 1 BOTTLE; Type 0: Not a Combination Product 6 NDC:11822-0612-6 2 in 1 CARTON 05/19/2020 05/19/2020 6 10 in 1 BLISTER PACK; Type 0: Not a Combination Product 7 NDC:11822-0612-7 1 in 1 CARTON 05/19/2020 7 300 in 1 BOTTLE; Type 0: Not a Combination Product 8 NDC:11822-0612-8 1 in 1 CARTON 04/25/2023 8 70 in 1 BOTTLE; Type 0: Not a Combination Product 9 NDC:11822-0612-9 1 in 1 CARTON 06/14/2023 9 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 10/21/2004 Labeler - Rite Aid Corporation (014578892)