Label: BERKLEY AND JENSEN ALLERGY RELIEF- loratadine tablet
- NDC Code(s): 68391-314-87, 68391-314-88
- Packager: BJWC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated March 28, 2025
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)Loratadine 10 mg
-
PurposeAntihistamine
-
Usestemporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose - • itchy, watery eyes - • sneezing - • itching of the nose or throat
-
WarningsDo not use - if you have ever had an allergic reaction to this product or any of its ingredients - Ask a doctor before use if you have - liver or kidney disease. Your doctor should determine if ...
-
Directionsadults and children 6 years and over - 1 tablet daily; not more than 1 tablet in 24 hours - children under 6 years of age - ask a doctor - consumers with liver or kidney disease - ask a ...
-
Other information• do not use if printed foil under cap is broken or missing - • store between 20° to 25°C (68° to 77°F)
-
Inactive ingredientslactose monohydrate, magnesium stearate, povidone, pregelatinized starch
-
Questions or comments?1-800-934-1204
-
Principal Display PanelCompare to the active ingredient in Claritin® berkley jensen® ORIGINAL PRESCRIPTION STRENGTH - 24 HOUR • NON-DROWSY* ALLERGY RELIEF - LORATADINE TABLETS, 10 mg - ANTIHISTAMINE - INDOOR & OUTDOOR ...
-
INGREDIENTS AND APPEARANCEProduct Information
