LORATADINE
-
loratadine solution
Silarx Pharmaceuticals, Inc
----------
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
Do not use if you have ever had allergic reaction to this product or any of it's 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.
adults and children 6 years and over | 2 teaspoonfuls daily; do not take more than 2 teaspoonfuls in 24 hours |
children 2 to under 6 years of age | 1 teaspoonful daily; do not take more than 1 teaspoonful in 24 hours |
children under 2 years of age | ask a doctor |
consumers with liver or kidney disease | ask a doctor |
Butylated hydroxylanisole, citric acid, glycerin, grape flavor, propylene glycol, purified water, sodium benzoate, sucralose.
1-888-974-5279
Manufactured by:
Silarx Pharmaceuticals, Inc.
19 West Street
Spring Valley, NY 10977 USA
Revised – August 2010
Severe Allergy Warning: Get emergency help immediately if you have hives along with any of the following symptoms:
These symptoms may be signs of anaphylactic shock. This condition can be life threatening if not treated by a health professional immediately. Symptoms of anaphylactic shock may occur when hives first appear or up to a few hours later.
Not a Substitute for Epinephrine. If your doctor has prescribed an epinephrine injector for “anaphylaxis” or severe allergy symptoms that could occur with your hives, never use this product as a substitute for the epinephrine injector. If you have been prescribed an epinephrine injector, you should carry it with you at all times.
- to prevent hives from any known cause such as:
because this product will not stop hives from occurring. Avoiding the cause of your hives is the only way to prevent them. Hives can sometimes be serious. If you do not know the cause of your hives, see your doctor for a medical exam. Your doctor may be able to help you find a cause.
- if you have ever had an allergic reaction to this product (loratadine) or any of its ingredients
Ask a doctor before use if you have
When using this product do not take more than directed. Taking more than directed may cause drowsiness.
adults and children 6 years and over | 2 teaspoonfuls daily; do not take more than 2 teaspoonfuls in 24 hours |
children under 6 years of age | ask a doctor |
consumers with liver or kidney disease | ask a doctor |
Butylated hydroxyanisole, citric acid, glycerin, grape flavor, propylene glycol, purified water, sodium benzoate, sucralose.
1-888-974-5279
Manufactured by:
Silarx Pharmaceuticals, Inc.
19 West Street
Spring Valley, NY 10977 USA
Revised – August 2010
Once Daily / Non-Drowsy*
Loratadine Oral Solution
Hives Relief
5 mg per 5 mL
Antihistamine
What you should know about:
Non- Drowsy*
Loratadine Oral Solution – Hives Relief
Original Prescription Strength – 24 Hour Product
Relief of Itching Due to Hives
(Please read all of this information before taking Loratadine Oral Solution – Hives Relief Product. Save this leaflet for future reference.)
What is Loratadine Oral Solution - Hives Relief product?
Loratadine Oral Solution - Hives Relief product contain loratadine, a non-drowsy *antihistamine.
Loratadine Oral Solution – Hives Relief Original prescription strength medicine to relieve itching due to hives. |
LORATADINE
loratadine solution |
||||||||||||||||||
|
||||||||||||||||||
|
||||||||||||||||||
|
||||||||||||||||||
|
||||||||||||||||||
|
Marketing Information | |||
Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
ANDA | ANDA077421 | 11/24/2010 |
LORATADINE
loratadine solution |
||||||||||||||||||
|
||||||||||||||||||
|
||||||||||||||||||
|
||||||||||||||||||
|
||||||||||||||||||
|
Marketing Information | |||
Marketing Category | Application Number or Monograph Citation | Marketing Start Date | Marketing End Date |
ANDA | ANDA077421 | 11/24/2010 |
Labeler - Silarx Pharmaceuticals, Inc (161630033) |
Revised: 06/2011 Silarx Pharmaceuticals, Inc