Choline Salicylate
Otinum is a Medication Indicated for Short-Term Use in Inflammatory Conditions of the External Auditory Canal Characterized by Pain, Itching, and Redness.
The Medication is also Recommended for Softening Earwax Before Ear Irrigation.
The Active Substance of Otinum Ear Drops is a Derivative of Salicylic Acid – Choline Salicylate.
Choline Salicylate Used Topically has Analgesic and Anti-Inflammatory Properties. This Reduces Pain and Inflammation in the Course of External Auditory Canal Inflammation.
The Glycerol Contained in the Medication Softens Earwax in the Ear, Making it Easier to Remove.
After Local Administration to the Ear, the Medication does not Have a Systemic Effect.
Eardrum Perforation may be Indicated by: Severe Ear Pain (Gradually Decreasing), Ringing in the Ears (Which may Indicate Damage to Deeper Ear Structures), Hearing Loss, Dizziness, and (or) Discharge from the Ear. The Causes of Eardrum Damage (Perforation) Include: Infections, Injuries (e.g., After Improper Ear Cleaning with Cotton Swabs), and Medical Reasons (e.g., Improper Ear Irrigation Due to Earwax).
Any Ear Pain is a Reason to Consult a Doctor.
The Medication Used to Treat Inflammatory Conditions of the External Auditory Canal Without Consulting a Doctor can be Used for a Short Period, not Longer than 3 Days. If There is no Improvement or Worsening of Symptoms Despite Using Otinum in the Recommended Doses for 3 Days, You Should Contact a Doctor.
If Additional Symptoms Appear, Indicating a Developing Disease Process (e.g., Fever, Malaise, Weakness, Dizziness, Discharge from the Ear), You Should Contact a Doctor.
In the Event of Recurrence of the Disease, the Use of Otinum Should be Decided by a Doctor.
Otinum may Mask Symptoms of Other Ear Diseases and Make their Proper Diagnosis Difficult or Delayed.
You Should Inform the Doctor About the Use of the Medication.
The Medication Contains a Preservative – Chlorobutanol Hemihydrate.
Otinum Should not be Used in a Manner Inconsistent with the Indications Listed in the Leaflet or with a Different Route of Administration (e.g., Orally, on Open Wounds, Especially in the Ear Canal or in the Eyes).
You Should Tell the Doctor or Pharmacist About all Medications Currently Used by the Patient or Recently Used, as well as Medications the Patient Plans to Use. This Applies to Over-the-Counter Medications as Well.
The Medication is Used Topically and does not Have a Systemic Effect.
Concomitant Use with Non-Steroidal Anti-Inflammatory Drugs (e.g., Aspirin, Ibuprofen) may Enhance Local Effects.
If the Patient is Pregnant or Breastfeeding, Suspects She may be Pregnant, or Plans to Have a Child, She Should Consult a Doctor or Pharmacist Before Using this Medication.
The Medication does not Affect the Ability to Drive Vehicles or Operate Machinery.
This Medication Should Always be Used Exactly as Described in the Patient Leaflet or as Directed by a Doctor or Pharmacist. In Case of Doubt, You Should Consult a Doctor or Pharmacist.
Otinum is Used Exclusively Topically, in the Ear.
Otinum is Intended for Use in Adults.
If You Feel that the Effect of Otinum is too Strong or too Weak, You Should Consult a Doctor.
Patients with Liver and (or) Kidney Function Disorders:
No Need to Change the Dosage.
It is Impossible to Overdose on the Medication by Administering it into the Ear.
Symptoms of Overdose that may Occur after Accidental Oral Ingestion of the Medication Include:
Disorientation, Dizziness, Excessive Sweating, Vomiting, Ringing in the Ears, and Too Rapid Breathing (Hyperventilation). In the Event of Ingesting Very Large Doses of the Medication, Central Nervous System Disorders may Occur, Including Breathing and Circulatory Disorders.
In the Event of Oral Ingestion of the Medication, You Should Immediately Consult a Doctor.
In the Event of Missing a Dose of the Medication at the Designated Time, You Should Administer it as Soon as Possible.
However, if the Time for the Next Dose is Approaching, You Should Omit the Missed Dose. You Should not Use a Double Dose to Make up for the Missed Dose.
Like all Medications, this Medication can Cause Undesirable Effects, although not Everybody will Experience them.
The Frequency of the Following Undesirable Effects is Unknown (Cannot be Determined from Available Data).
Local Allergic Reactions (Redness and Itching of the Skin).
In Patients with Eardrum Perforation During the Use of the Medication, Hearing Loss may Occur.
If You Experience any Undesirable Effects, Including any Undesirable Effects not Listed in the Leaflet, You Should Inform the Doctor, Pharmacist, or Nurse. Undesirable Effects can be Reported Directly to the Department of Monitoring of Adverse Reactions to Medicinal Products of the Office for Registration of Medicinal Products, Medical Devices, and Biocidal Products, Al. Jerozolimskie 181C, 02-222 Warsaw, Tel.: +48 22 49 21 301, Fax: +48 22 49 21 309, Website: https://smz.ezdrowie.gov.pl.
Reporting Undesirable Effects will Allow for More Information to be Collected on the Safety of the Medication.
The Medication Should be Stored in a Place Invisible and Inaccessible to Children.
Do not Store at a Temperature Above 25°C. Store in the Original Packaging.
Do not Use this Medication after the Expiration Date Stated on the Packaging. The Expiration Date Refers to the Last Day of the Specified Month.
Medications Should not be Disposed of in Sewers or Household Waste Containers. You Should Ask the Pharmacist how to Dispose of Medications that are no Longer Used. This will Help Protect the Environment.
The Medication Packaging is a 10 ml PE Bottle with a Dropper and a Screw Cap with a Guarantee Ring, in a Cardboard Box. The Packaging Contains 10 g of the Medication.
Viatris Healthcare Limited
Damastown Industrial Park
Mulhuddart
Dublin 15, Dublin, Ireland
ICN Polfa Rzeszów S.A.
ul. Przemysłowa 2
35-959 Rzeszów
Poland
InPharm Sp. z o.o.
ul. Strumykowa 28/11
03-138 Warsaw
InPharm Sp. z o.o. Services sp. k.
ul. Chełmżyńska 249
04-458 Warsaw
Lithuanian, Country of Export Marketing Authorization Number:LT/1/94/1929/001
Parallel Import License Number:153/15
[Information about the Trademark]
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