Label: NON-DROWSY ALLERGY RELIEF- loratadine tablet tablet
- NDC Code(s): 66715-8815-6
- Packager: Lil' Drug Store Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated August 17, 2023
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
-
Warnings
Warnings
Do not use
Do not use if you have ever had an allergic reaction to this product or any of its ingredients
Ask a doctor before use if you have
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
When using this product do not take more than directed. Taking more than directed may cause drowsiness.
- Directions
- Other Information
- Inactive Ingredients
-
Non-Drowsy Allergy Relief, 24/7 Life by 7-ELEVEN 6ct, PDP/Package
24/7 Life BY 7-ELEVEN TM
Original Prescription
Strength
Non-Drowsy*
AllergyRelief
Loratadine Tablets, 10 mg
Antihistamine
Indoor & Outdoor Allergies
24 Hour Relief of:Sneezing, Runny Nose,
Itchy, Watery Eyes,
Itchy Throat or Nosecompare to
Claritin ® Tablets
active ingredient*
*When taken as directed.
See Drug Facts Panel.
6
TABLETS
[tablet image]
Actual Size
-
INGREDIENTS AND APPEARANCE
NON-DROWSY ALLERGY RELIEF
loratadine tablet tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:66715-8815 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 MAGNESIUM STEARATE (UNII: 70097M6I30) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) Product Characteristics Color white Score no score Shape OVAL Size 8mm Flavor Imprint Code LOR;10;APO Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:66715-8815-6 1 in 1 CARTON 05/06/2022 1 6 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 ANDA076471 05/06/2022 Labeler - Lil' Drug Store Products, Inc. (093103646)