Label: ALLERGY RELIEF- loratadine tablet
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NDC Code(s):
59779-612-03,
59779-612-39,
59779-612-46,
59779-612-49, view more59779-612-58, 59779-612-60, 59779-612-65, 59779-612-70, 59779-612-72, 59779-612-75, 59779-612-76, 59779-612-88, 59779-612-95
- Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 9, 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
VALUE SIZE
CVS Health
Compare to the active ingredient in Claritin® Tablets
Indoor & Outdoor Allergies
Original Prescription Strength
Non-Drowsy*
24 HOUR
Allergy Relief
LORATADINE TABLETS, 10 mg
Antihistamine
24 hour relief of:
Sneezing
Itchy, watery eyes
Runny nose
Itchy throat or nose
Actual Size
365 TABLETS
*When taken as directed.
See Drug Facts Panel.
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-612 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:59779-612-46 10 in 1 CARTON 01/28/2009 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:59779-612-72 1 in 1 CARTON 05/28/2009 08/31/2021 2 60 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:59779-612-75 1 in 1 CARTON 05/08/2009 3 90 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:59779-612-58 1 in 1 CARTON 07/26/2007 07/26/2007 4 40 in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:59779-612-39 30 in 1 CARTON 01/04/2005 5 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 6 NDC:59779-612-70 2 in 1 CARTON 09/04/2015 6 NDC:59779-612-76 120 in 1 BOTTLE; Type 0: Not a Combination Product 7 NDC:59779-612-95 1 in 1 CARTON 09/14/2015 7 45 in 1 BOTTLE; Type 0: Not a Combination Product 8 NDC:59779-612-49 40 in 1 CARTON 12/13/2015 09/30/2021 8 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 9 NDC:59779-612-03 1 in 1 CARTON 10/10/2017 9 70 in 1 BOTTLE; Type 0: Not a Combination Product 10 NDC:59779-612-88 365 in 1 BOTTLE; Type 0: Not a Combination Product 03/23/2018 11 NDC:59779-612-65 1 in 1 CARTON 04/03/2018 11 30 in 1 BOTTLE; Type 0: Not a Combination Product 12 NDC:59779-612-60 20 in 1 CARTON 07/21/2009 12 1 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 ANDA ANDA076301 01/04/2005 Labeler - CVS Pharmacy (062312574)