Label: ALL DAY ALLERGY RELIEF- loratadine tablet
- NDC Code(s): 59726-758-10
- Packager: P & L Development, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated October 26, 2021
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
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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?
-
Principal Display Panel
Compare to the active ingredient in Claritin®†
all day allergy relief
loratadine tablets 10 mg
non-drowsy*
Indoor & Outdoor Allergies
24 hour relief of:
- sneezing
- runny nose
- itchy, watery eyes
- itchy throat or nose
gluten-free
*when taken as directed, see drug facts panel.
tablets
†This product is not manufactured or distributed by Bayer Healthcare LLC, distributor of Claritin®.
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:
PL Developments
200 Hicks Street
Westbury, NY 11590
- Package Label
-
INGREDIENTS AND APPEARANCE
ALL DAY ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59726-758 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 GG296 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59726-758-10 10 in 1 CARTON 09/30/2018 07/26/2024 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 09/30/2018 07/26/2024 Labeler - P & L Development, LLC (800014821)