The following Structured Product Label (SPL) was submitted to the FDA by Viatris Specialty Llc for the product Urelle (NDC 0037-6321). 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 description:, indications and usage:, contraindications:, warnings:, precautions:, drug interactions:, additional information for healthcare professionals:, adverse reactions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Urelle® tablets for oral administration are supplied as navy blue round tablets with “A-002” debossed on one side.
Each Tablet Contains:
Hyoscyamine Sulfate 0.12 mg
Methenamine 81.0 mg
Methylene Blue 10.8 mg
Phenyl Salicylate 32.4 mg
Sodium Phosphate Monobasic 40.8 mg
INACTIVE INGREDIENTS:
Corn Starch, Dicalcium Phosphate, FD&C Blue #2/Indigo Carmine Aluminum Lake, Magnesium Stearate, Microcrystalline Cellulose, Polyethylene Glycol, Polyvinyl Alcohol, Talc, Titanium Dioxide.
Urelle® is indicated for the treatment of symptoms of irritative voiding. Indicated for the relief of local symptoms, such as inflammation, hypermotility, and pain, which accompany lower urinary tract infections. Indicated for the relief of urinary tract symptoms caused by diagnostic procedures.
Hypersensitivity to any of the ingredients is possible. Risk - benefit should be carefully considered when the following medical problems exist: cardiac disease (especially cardiac arrhythmias, congestive heart failure, coronary heart disease, mitral stenosis); gastrointestinal tract obstructive disease; glaucoma; myasthenia gravis; acute urinary retention may be precipitated in obstructive uropathy (such as bladder neck obstruction due to prostatic hypertrophy).
If rapid pulse, dizziness, or blurring of vision occurs, discontinue use immediately.
Patients should be advised that urine will be colored blue when taking this medication. Do not exceed recommended dosage.
Cross sensitivity and/or related problems - patients intolerant of belladonna alkaloids or salicylates may be intolerant of this medication also. Delay in gastric emptying could complicate the management of gastric ulcers.
Urelle® contains methylene blue. Methylene blue should generally NOT be given to patients taking serotonergic drugs.
Although the exact mechanism of this drug interaction is unknown, methylene blue inhibits the action of monoamine oxidase A— an enzyme responsible for breaking down serotonin in the brain. It is believed that when methylene blue is given to patients taking serotonergic psychiatric medications, high levels of serotonin can build up in the brain, causing toxicity. This is referred to as Serotonin Syndrome. Signs and symptoms of Serotonin Syndrome include mental changes (confusion, hyperactivity, memory problems), muscle twitching, excessive sweating, shivering or shaking, diarrhea, trouble with coordination, and/or fever.
Methylene blue can interact with serotonergic psychiatric medications and cause serious CNS toxicity.
In emergency situations requiring life-threatening or urgent treatment with methylene blue (as described above), the availability of alternative interventions should be considered and the benefit of methylene blue treatment should be weighed against the risk of serotonin toxicity. If methylene blue must be administered to a patient receiving a serotonergic drug, the serotonergic drug must be immediately stopped, and the patient should be closely monitored for emergent symptoms of CNS toxicity for two weeks (five weeks if fluoxetine [Prozac] was taken), or until 24 hours after the last dose of methylene blue, whichever comes first.
In non-emergency situations when non-urgent treatment with methylene blue is contemplated and planned, the serotonergic psychiatric medication should be stopped to allow its activity in the brain to dissipate. Most serotonergic psychiatric drugs should be stopped at least 2 weeks in advance of methylene blue treatment. Fluoxetine (Prozac), which has a longer half-life compared to similar drugs, should be stopped at least 5 weeks in advance.
Treatment with the serotonergic psychiatric medication may be resumed 24 hours after the last dose of methylene blue.
Serotonergic psychiatric medications should not be started in a patient receiving methylene blue. Wait until 24 hours after the last dose of methylene blue before starting the antidepressant.
Educate your patients to recognize the symptoms of serotonin toxicity or CNS toxicity and advise them to contact a healthcare professional immediately if they experience any symptoms while taking serotonergic psychiatric medications or methylene blue.
To report SUSPECTED ADVERSE REACTIONS, contact Meda Pharmaceuticals Inc. at 1-877-999-8402 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Adults – One tablet orally 4 times per day followed by liberal fluid intake.
Pediatric – Dosage must be individualized by a physician for older children. Urelle® is not recommended for use in children 6 years of age or younger.
Urelle® tablets for oral administration are supplied in child resistant bottles of 90 tablets (NDC 0037-6321-90).
Store at controlled room temperature 20°-25°C (68°-77°F).
Dispense in a tight, light resistant container as defined in the USP.
KEEP THIS AND ALL DRUGS OUT OF THE REACH OF CHILDREN.
Distributed by:
Meda Pharmaceuticals®
Somerset, New Jersey 08873-4120
© 2014 Meda Pharmaceuticals Inc.
MEDA PHARMACEUTICALS and URELLE are registered trademarks of Meda AB or a related entity.
Rx Only
IN-632110-01
Rev. 07/2014
NDC 0037-6321-90
90 TABLETS
Urelle®
Urinary Antiseptic
Rx only
Distributed by:
MEDA
PHARMACEUTICALS®
Somerset, New Jersey 08873-4120
© 2018 Meda Pharmaceuticals Inc.
MEDA PHARMACEUTICALS® and URELLE® are
registered trademarks of Meda AB or a related entity.
Description: Urelle® tablets for oral administration are supplied as navy blue
round tablets with “A-002” debossed on one side.
Each Tablet Contains:
Hyoscyamine Sulfate 0.12 mg
Methenamine 81.0 mg
Methylene Blue 10.8 mg
Phenyl Salicylate 32.4 mg
Sodium Phosphate Monobasic 40.8 mg
Dosage: Adults - one tablet orally 4 times per day followed by liberal fluid intake.
Pediatric - Dosage must be individualized by a physician for older children.
Urelle® is not recommended for use in children 6 years of age or younger.
Precaution: Contains Methylene Blue and should NOT be taken with serotonergic
psychiatric medications. For full product information see package insert.
To report SUSPECTED ADVERSE REACTIONS, contact Meda Pharmaceuticals
Inc. at 1-877-999-8402 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.
Storage: Store at controlled room temperature 20°-25°C (68°-77°F). Dispense
in a tight, light resistant container as defined in the USP.
KEEP OUT OF THE REACH OF CHILDREN.
Note: Patients should be advised that urine will be colored blue when taking
this medication.
LB-632110-02 Rev. 02/2018
Urelle Antiseptic Label (Image 01)
* Please review the disclaimer below.
