Label: ALLERGY RELIEF- loratadine capsule, liquid filled
- NDC Code(s): 83324-103-10
- Packager: CHAIN DRUG MARKETING ASSOCIATION, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated August 12, 2024
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- SPL UNCLASSIFIED SECTION
- Active Ingredient (in each capsule)
- Purpose
- Uses
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Warnings
Do not useif you have ever had an allergic reaction to this product or any of its ingredients.
Ask a doctor before use if you haveliver or kidney disease. Your doctor should determine if you need a different dose.
When using this productdo 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
QUALITY CHOICE®
NDC 83324-103-10
†Compare to Active Ingredient in CLARITIN® Liqui-Gels®
Non-Drowsy*
Allergy Relief 24 Hour
Loratadine 10 mg
Antihistamine
Indoor & Outdoor Allergies
For Relief of:
Sneezing | Runny Nose
Itchy, Watery Eyes | Itchy Throat or Nose
*When taken as directed. See Drug Facts Panel.
Actual Size
10 SOFTGELS** **Liquid-Filled Capsules
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INGREDIENTS AND APPEARANCE
ALLERGY RELIEF
loratadine capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83324-103 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 FD&C BLUE NO. 1 (UNII: H3R47K3TBD) GELATIN (UNII: 2G86QN327L) CAPRIC ACID (UNII: 4G9EDB6V73) POVIDONE K30 (UNII: U725QWY32X) WATER (UNII: 059QF0KO0R) SORBITOL (UNII: 506T60A25R) POLYSORBATE 80 (UNII: 6OZP39ZG8H) SORBITAN (UNII: 6O92ICV9RU) Product Characteristics Color blue (Light Blue) Score no score Shape OVAL (oval shaped) Size 3mm Flavor Imprint Code 21 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83324-103-10 1 in 1 CARTON 08/12/2024 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 ANDA206214 08/12/2024 Labeler - CHAIN DRUG MARKETING ASSOCIATION, INC. (011920774)