Label: DG HEALTH ALLERGY RELIEF- loratadine tablet
- NDC Code(s): 55910-806-39, 55910-806-49, 55910-806-65, 55910-806-72
- Packager: Dolgencorp Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated October 27, 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
-
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
DG™|health
Compare to the active ingredient of Claritin® Tablets
Original Prescription Strength
Allergy Relief
Loratadine Tablets, 10 mg • Antihistamine
Indoor & Outdoor Allergies
24 HOUR
Non Drowsy*
24 Hour Relief of:
• Sneezing • Runny nose
• Itchy, watery eyes
• Itchy throat or nose
10 mg
*When taken as directed. See Drug Facts Panel.
30 Tablets
Actual Tablet Size
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INGREDIENTS AND APPEARANCE
DG HEALTH ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-806 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:55910-806-39 30 in 1 CARTON 04/18/2012 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:55910-806-72 1 in 1 CARTON 04/13/2012 2 60 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:55910-806-49 40 in 1 CARTON 04/18/2012 3 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 4 NDC:55910-806-65 1 in 1 CARTON 04/28/2023 4 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 04/13/2012 Labeler - Dolgencorp Inc (068331990)