Label: ALLERGY RELIEF- loratadine tablet
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NDC Code(s):
41250-612-03,
41250-612-39,
41250-612-49,
41250-612-65, view more41250-612-72, 41250-612-76, 41250-612-87
- Packager: Meijer Distribution Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 11, 2023
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
Compare to Claritin® active ingredient
NON-DROWSY*
allergy relief
Loratadine Tablets 10 mg
Antihistamine
INDOOR & OUTDOOR ALLERGIES
24 HOUR RELIEF OF:
Sneezing; Runny Nose; Itchy, Watery Eyes; Itchy Throat or Nose
ORIGINAL PRESCRIPTION STRENGTH
70 Tablets | actual size
*When taken as directed. See Drug Facts Panel.
70 Days of Relief
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-612 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:41250-612-39 30 in 1 CARTON 06/13/2007 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:41250-612-72 1 in 1 CARTON 06/22/2007 05/05/2015 2 60 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:41250-612-76 1 in 1 CARTON 06/29/2007 3 120 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:41250-612-87 1 in 1 CARTON 04/18/2007 4 300 in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:41250-612-03 1 in 1 CARTON 10/02/2013 5 70 in 1 BOTTLE; Type 0: Not a Combination Product 6 NDC:41250-612-49 40 in 1 CARTON 02/27/2014 6 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 7 NDC:41250-612-65 1 in 1 CARTON 05/11/2023 7 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 04/18/2007 Labeler - Meijer Distribution Inc (006959555)