Active Ingredient (In Each Tablet)
Loratadine, USP 10 mg
Sunmark Loratadine Odt
FDA Label NDC 49348-930
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sunmark for the product Sunmark Loratadine Odt (NDC 49348-930). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, uses, do not use, ask a doctor before use if you have, when using this product, stop use and ask a doctor if, if pregnant or breast-feeding,, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antihistamine
Uses
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- runny nose
- itchy, watery eyes
- sneezing
- itching of the nose or throat
Do 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 you need a different dose.
When Using This Product
do not take more than directed. Taking more than directed may cause drowsiness.
Stop Use And Ask A Doctor If
an allergic reaction to this product occurs. Seek medical help right away.
If Pregnant Or Breast-Feeding,
ask a health professional before use.
Keep Out Of Reach Of Children.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Directions
- 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
Other Information
- 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.
Inactive Ingredients
aspartame, croscarmellose sodium, fruit flavors, magnesium stearate, mannitol, sodium stearyl fumarate
Questions?
call 1-800-406-7984
Keep the carton. It contains important information.
See end panel for expiration date.
Distributed by McKesson
One Post Street, San Francisco, CA 94104
www.sunmarkbrand.com
Principal Display Panel
sunmark®
NDC 49348-930-01
allergy relief
24 HOUR
loratadine Orally Disintegrating Tablets, 10 mg
Antihistamine
For adults and children six years and older
Indoor & Outdoor Allergies
Non-drowsy*
Relief of sneezing; runny nose; itchy, watery eyes; itchy throat or nose
MELTS IN YOUR MOUTH
10 ORALLY DISINTEGRATING TABLETS
*When taken as directed.
See Drug Facts Panel.
COMPARE TO CLARITIN®REDITABS®ACTIVE INGREDIENT†
†The product is not manufactured or distributed by Schering-Plough Healthcare Products , Inc.
CLARITIN®and REDITABS®are registered trademarks of Schering Corporation.
This Is The 10 Count Blister Carton Label For Sunmark Loratadine Odt, 10 mg. (Lora Odt)
sunmark®
NDC 49348-929-04
allergy relief
24 HOUR
Loratadine Orally Disintegrating Tablets, 10 mg
Antihistamine
For adults and children six years and older
Indoor & Outdoor Allergies
Non-drowsy*
Relief of sneezing; runny nose; itchy, watery eyes; itching of nose & throat
MELTS IN YOUR MOUTH
24 ORALLY DISINTEGRATING TABLETS
*When taken as directed.
See Drug Facts Panel.
COMPARE TO ALAVERT®ACTIVE INGREDIENT†
†The product is not manufactured or distributed by Wyeth Consumer Healthcare, owner of the registered trademark Alavert®.
This Is The 24 Count Blister Carton Label For Sunmark Loratadine Odt (alavert). (Lora Alavert)
* Please review the disclaimer below.
