Label: ALL DAY ALLERGY RELIEF- loratadine tablet
- NDC Code(s): 83324-147-10
- Packager: QUALITY CHOICE (Chain Drug Marketing Association)
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 16, 2024
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- 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 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 Eye | 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 CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOW ANY SIGN OF TAMPERING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION
Distributed by: CDMA, Inc.
Novi, MI 48375
- Package Label
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INGREDIENTS AND APPEARANCE
ALL DAY ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83324-147 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:83324-147-10 10 in 1 CARTON 07/31/2024 1 1 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 ANDA075209 07/31/2024 Labeler - QUALITY CHOICE (Chain Drug Marketing Association) (011920774)