Label: ALL DAY ALLERGY RELIEF- loratadine tablet
- NDC Code(s): 83324-146-30
- Packager: QUALITY CHOICE (Chain Drug Marketing Association)
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated June 17, 2024
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® 24 Hour
Original Prescription Strength
Allergy Relief
Loratadine 10 mg tablets
Antihistamine
Indoor & Outdoor Allergies
Relief of:
- Sneezing | Runny nose
- Itchy, watery eyes
- Itchy throat or nose
Gluten-Free
24 Hour Allergy Relief
Non-Drowsy
TABLETS
*when taken as directed, see drug facts panel
†This product is not manufactured or distributed by Bayer Healthcare LLC, distributor of Claritin® 24 Hour
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION
Distributed by CDMA, Inc.
Novi, MI 48375
- Package Label
-
INGREDIENTS AND APPEARANCE
ALL DAY ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83324-146 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) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SODIUM STARCH GLYCOLATE TYPE A CORN (UNII: AG9B65PV6B) Product Characteristics Color white Score no score Shape ROUND Size 6mm Flavor Imprint Code 439 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83324-146-30 1 in 1 BOX 07/31/2024 1 30 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA075209 07/31/2024 Labeler - QUALITY CHOICE (Chain Drug Marketing Association) (011920774)