Loratadine ODT by Topco Associates LLC
Dosage form: tablet, orally disintegrating
Ingredients: LORATADINE 10mg
Labeler: Topco Associates LLC
NDC Code: 36800-528
Loratadine USP, 10 mg
Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- runny nose
- itchy, watery eyes
- itching of the nose or throat
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 right away (1-800-222-1222).
- place 1 tablet on tongue; tablet disintegrates, with or without water
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
- Phenylketonurics: Contains Phenylalanine 0.6 mg Per Tablet.
- TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
- store between 20° to 25° C (68° to 77° F). Protect from excessive moisture.
- keep in a dry place.
- use tablet immediately after opening individual blister.
Aspartame, croscarmellose sodium, magnesium stearate, mannitol, mint flavor, sodium stearyl fumarate, strawberry cream flavor, tutti-frutti flavor
Ages 6 years and older
Children's MELT-IN-YOUR-MOUTH TABLETS. NO WATER NEEDED
Original Prescription Strength
24 HOUR NON-DROWSY*
LORATADINE ORALLY DISINTEGRATING TABLETS, USP 10 mg
Indoor & Outdoor Allergies
For 24 Hour Relief of:
- Runny Nose
- Itchy, Watery Eyes
- Itchy Throat or Nose
COMPARE TO CLARITIN®REDITABS®active ingredient†
10 ORALLY DISINTEGRATING TABLETS
*When taken as directed. See Drug Facts Panel.
DISTRIBUTED BY TOPCO ASSOCIATES LLC
loratadine tablet, orally disintegrating
|Labeler - Topco Associates LLC (006935977)|
|Registrant - Ranbaxy Pharmaceuticals Inc. (937890044)|
|Ohm Laboratories Inc.||184769029||manufacture(36800-528)|
Medically reviewed on Apr 4, 2018
Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.