Indications and uses
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat
adults 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 doctor
Loratadine, USP 10 mg
Antihistamine
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
if you have ever had an allergic reaction to this product or any of its ingredients.
liver or kidney disease. Your doctor should determine if you need a different dose.
do not take more than directed. Taking more than directed may cause drowsiness.
an allergic reaction to this product occurs. Seek medical help right away.
ask a health professional before use.
In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
| adults 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 doctor |
lactose monohydrate, magnesium stearate, microcrystalline cellulose, sodium starch glycolate
Call 1-877-753-3935 Monday-Friday 9AM-5PM EST
Compare to the active ingredient in Claritin® 24 Hour†
Indoor & Outdoor Allergies
Non-Drowsy*
Allergy Relief
LORATADINE
TABLETS, 10 mg
Antihistamine
24 hour relief of:
*When taken as directed, See Drug Facts Panel.
TABLETS
†This product is not manufactured or distributed by Bayer Healthcare LLC, distributor of Claritin® 24 Hour
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION
Distributed by:
CVS Pharmacy, Inc.
One CVS Drive
Woonsocket, RI 02895
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 51316-915 | 51316-915-30 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| LORATADINE | 7AJO3BO7QN | ACTIB |
| LACTOSE MONOHYDRATE | EWQ57Q8I5X | IACT |
| MAGNESIUM STEARATE | 70097M6I30 | IACT |
| MICROCRYSTALLINE CELLULOSE | OP1R32D61U | IACT |
| SODIUM STARCH GLYCOLATE TYPE A CORN | AG9B65PV6B | IACT |
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 73df1add-f75b-4fd2-a9a3-c30d94fb5d2d | 647484e5-dd05-46fa-843f-4caea1e7dc77 | 2025-01-28 | Warnings | 647484e5-dd05-46fa-843f-4caea1e7dc77 |
Adverse event summaries are temporarily unavailable. Other product information remains available.