Label: EQUATE ALLERGY RELIEF- loratadine tablet
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NDC Code(s):
49035-612-46,
49035-612-47,
49035-612-65,
49035-612-72, view more49035-612-76, 49035-612-87, 49035-612-95
- Packager: Wal-Mart Stores Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated December 5, 2022
If you are a consumer or patient 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
equate™
CONVENIENT BOTTLE
Compare to Claritin® Tablets Active Ingredient
Non-Drowsy*
Allergy Relief
Loratadine Tablets, 10 mg/Antihistamine
Indoor and Outdoor Allergies
Relief of:
Sneezing
Runny nose
Itchy, watery eyes
Itchy throat or nose
24 HOUR
Original Prescription Strength
*When taken as directed.
See Drug Facts Panel.
10 mg
60 TABLETS
Actual Size
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INGREDIENTS AND APPEARANCE
EQUATE ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-612 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:49035-612-72 1 in 1 CARTON 04/27/2007 1 60 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49035-612-65 1 in 1 CARTON 02/29/2012 04/08/2015 2 30 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:49035-612-87 2 in 1 PACKAGE 03/01/2012 3 150 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:49035-612-46 10 in 1 CARTON 02/28/2012 4 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 5 NDC:49035-612-95 1 in 1 CARTON 08/20/2013 5 45 in 1 BOTTLE; Type 0: Not a Combination Product 6 NDC:49035-612-76 2 in 1 CARTON 02/03/2015 01/18/2019 6 60 in 1 BOTTLE; Type 0: Not a Combination Product 7 NDC:49035-612-47 150 in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2012 09/01/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076301 04/27/2007 Labeler - Wal-Mart Stores Inc (051957769)