Label: ALLERGY RELIEF- loratadine capsule, liquid filled
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Contains inactivated NDC Code(s)
NDC Code(s): 11822-2022-3 - Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 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 capsule)
- 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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SPL UNCLASSIFIED SECTION
†This product is not manufactured or distributed by the owners of Claritin® LIQUI-GELS®.
THIS PRODUCT IS PACKAGED IN A CHILD-RESISTANT AND TAMPER EVIDENT PACKAGE. USE ONLY IF BLISTERS ARE INTACT.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.DO NOT USE IF CARTON IS OPEN, OR IF INDIVIDUAL BLISTER UNIT IS OPEN OR TORN
*WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL
DISTRIBUTED BY:
RITE AID, 30 HUNTER LANE,
CAMP HILL, PA17011
www.riteaid.com
SATISFACTION
GUARANTEE
If you're not satisfied, we'll
happily refund your money.
Lot#
Expiration Date
Rev# 04/21
L0000439
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Principal Display Panel
NDC 11822-2022-3
Original Prescription Strength
†Compare to the active ingredient in Claritin® Liqui-Gels®*
ALLERGY RELIEF
LORATADINE CAPSULES, 10 mg
ANTIHISTAMINE
NON-DROWSY*
INDOOR/OUTDOOR ALLERGIES
24 HOUR RELIEF OF
Sneezing • Runny nose • Itchy, watery eyes
Itchy throat or nose
Actual Size
10 SOFTGELS**
(1X10) (**LIQUID-FILLED CAPSULES)
*WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
loratadine capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-2022 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 CAPRYLIC/CAPRIC MONO/DI-GLYCERIDES (UNII: U72Q2I8C85) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) GELATIN (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) HYPROMELLOSES (UNII: 3NXW29V3WO) HYDROLYSED BOVINE COLLAGEN (ENZYMATIC; 2000-5000 MW) (UNII: 5WE8P977RQ) ISOPROPYL ALCOHOL (UNII: ND2M416302) MANNITOL (UNII: 3OWL53L36A) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SORBITAN (UNII: 6O92ICV9RU) SORBITOL (UNII: 506T60A25R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color blue Score no score Shape OVAL Size 10mm Flavor Imprint Code L10 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-2022-3 1 in 1 CARTON 06/01/2021 1 10 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 ANDA202538 06/01/2021 Labeler - Rite Aid Corporation (014578892) Registrant - Bionpharma Inc. (079637826) Establishment Name Address ID/FEI Business Operations Patheon Softgels Inc. 002193829 manufacture(11822-2022)