Label: SOUND BODY ALLERGY RELIEF- loratadine tablet
- NDC Code(s): 50594-010-39, 50594-010-46, 50594-010-75, 50594-010-87
- Packager: Big Lots Stores, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated January 9, 2020
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
-
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?
-
Principal Display Panel
Compare to the Active Ingredient in Claritin® Tablets
NON-DROWSY*
Original Prescription Strength
Allergy Relief
Loratadine Tablets, 10 mg
Antihistamine
*When taken as directed. See Drug Facts Panel.
Indoor & Outdoor Allergies
24 HOUR RELIEF OF: Sneezing; Runny Nose;
Itchy, Watery Eyes; Itchy Throat or Nose
30 TABLETS
Actual Size
24 HOUR
-
INGREDIENTS AND APPEARANCE
SOUND BODY ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50594-010 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:50594-010-46 10 in 1 CARTON 06/12/2015 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:50594-010-39 30 in 1 CARTON 03/29/2016 2 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:50594-010-75 1 in 1 CARTON 03/18/2019 3 90 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:50594-010-87 1 in 1 CARTON 01/09/2020 4 300 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 06/12/2015 Labeler - Big Lots Stores, Inc. (017885351)