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Medicine overview

Indications of Tearon 0.4%+0.3%

Tearon 0.4%+0.3% is indicated for the temporary relief of burning, irritation, and discomfort due to dryness of the eye (dry eye syndrome). It is used as an ophthalmic lubricant/artificial tear product.

  • Established use: Symptomatic relief of dry eye symptoms such as burning, stinging, itching, and foreign body sensation caused by exposure to wind, sun, or other mild irritants, and reduced or deficient tear production.
  • Established use: Protection of the eye against further irritation and as a lubricant to prevent dryness during activities that reduce blinking (e.g., prolonged reading, computer use).
  • Adjunct use: Supportive lubrication for eyes after ophthalmic examinations or minor ocular surface irritation, as advised by a physician.

Tearon 0.4%+0.3% is an over-the-counter product intended for symptomatic relief and does not treat the underlying cause of dry eye.

Composition

Each mL of ophthalmic solution contains Polyethylene Glycol 400 0.4% w/v and Propylene Glycol 0.3% w/v as active lubricating agents, in a sterile ophthalmic base.

Description

Tearon 0.4%+0.3% is a combination ophthalmic lubricant (artificial tear) formulation used for the temporary relief of dry eye symptoms. Polyethylene glycol and propylene glycol are both demulcent, water-soluble lubricants that coat the ocular surface, increase tear film stability, and reduce friction between the eyelid and cornea during blinking.

Tearon 0.4%+0.3% is available as eye drops and, in some formulations, as an ophthalmic gel, and is widely marketed in Bangladesh as an over-the-counter dry eye/lubricant product.

Theropeutic Class

Tearon 0.4%+0.3% belongs to the therapeutic class of ophthalmic lubricants and tear substitutes (drugs for dry eyes).

Pharmacology

Tearon 0.4%+0.3% works through a demulcent and lubricating mechanism rather than a systemic pharmacologic action. Polyethylene glycol 400 and propylene glycol are viscosity-enhancing, water-retaining agents that form a smooth, lubricating film over the surface of the eye.

Some formulations of Tearon 0.4%+0.3% contain a gelling agent that reacts with the electrolyte composition of natural tears to form a transient, adaptive gel matrix on the ocular surface, which prolongs contact time, stabilizes the tear film, protects against further moisture loss, and supports the natural repair of the corneal epithelium.

Dosage & Administration of Tearon 0.4%+0.3%

Adults

Instill 1 to 2 drops of Tearon 0.4%+0.3% into the affected eye(s) as needed, or as directed by the physician. When used regularly for chronic dry eye, a typical regimen is 1 drop up to 4 times daily.

Administration Instructions

  • Wash hands before use.
  • Tilt the head back, pull down the lower eyelid to form a pocket, and instill the drop(s).
  • Avoid touching the dropper tip to the eye, fingers, or any other surface to prevent contamination of the solution.
  • Replace the cap tightly after each use.
  • If wearing contact lenses, remove them before instillation unless the product is specifically labeled as safe for use with contact lenses in place; consult the product label or a physician.
  • If using another eye medication concurrently, wait at least 5 minutes between products.

Dosage of Tearon 0.4%+0.3%

1 to 2 drops of Tearon 0.4%+0.3% in the affected eye(s) as needed, up to 4 times daily, or as directed by a physician.

Administration of Tearon 0.4%+0.3%

For topical ophthalmic (eye) use only. Instill directly into the conjunctival sac of the affected eye(s), avoiding contact between the dropper tip and the eye or other surfaces.

Interaction of Tearon 0.4%+0.3%

Tearon 0.4%+0.3% is a topical ophthalmic product with minimal systemic absorption, so clinically significant drug-drug interactions are not well established.

  • If using other topical ophthalmic medications (e.g., other eye drops), separate administration by at least 5 minutes to prevent one product from washing out another and to allow adequate absorption of each.
  • No significant interactions with systemic medications have been documented.

Contraindications

Tearon 0.4%+0.3% is contraindicated in patients with known hypersensitivity to polyethylene glycol, propylene glycol, or any other ingredient in the formulation.

Side Effects of Tearon 0.4%+0.3%

Tearon 0.4%+0.3% is generally well tolerated. Reported adverse effects are typically mild and localized to the eye:

  • Transient blurred vision immediately after instillation
  • Mild eye irritation, stinging, or burning on instillation
  • Ocular discomfort or foreign body sensation
  • Hypersensitivity reactions (redness, itching, swelling) in sensitive individuals — see Contraindications

If irritation worsens, persists, or is accompanied by eye pain, vision changes, or redness lasting more than 72 hours, discontinue use and consult a physician.

Pregnancy & Lactation

There are no well-controlled studies of Tearon 0.4%+0.3% use in pregnant or breastfeeding women; however, as a topical ophthalmic lubricant with minimal systemic absorption, significant fetal or infant risk is not expected. As with any medication, Tearon 0.4%+0.3% should be used during pregnancy and lactation only if clearly needed, and a physician or pharmacist should be consulted before use.

Precautions & Warnings

The following precautions apply to the use of Tearon 0.4%+0.3%:

  • For topical ocular use only. Not for injection or oral use.
  • Do not use if the solution changes color or becomes cloudy.
  • Avoid touching the dropper tip to the eye, fingers, or any surface to prevent contamination of the product.
  • Remove contact lenses before instillation unless the specific product is labeled safe for use with lenses in place.
  • Discard the container one month after first opening, or as specified on the product label, to reduce the risk of contamination.
  • Discontinue use and seek medical evaluation if eye pain develops, vision changes occur, or redness/irritation persists or worsens — these may indicate a condition unrelated to simple dry eye.
  • Preservative-containing formulations may cause sensitivity with prolonged or frequent use; preservative-free single-use formulations are available for sensitive patients or frequent daily use.
  • Keep out of reach of children.

Overdose Effects of Tearon 0.4%+0.3%

Ocular overdose (excessive instillation) of Tearon 0.4%+0.3% is unlikely to cause serious harm and may cause transient blurred vision or watering of the eye; excess solution should be gently wiped away. If accidentally ingested, or if a large amount is instilled and irritation or other symptoms occur, seek immediate medical attention or contact a poison control center.

Storage Conditions

Store at room temperature (below 30°C), away from light and moisture. Keep out of reach of children. Discard the container one month after first opening unless otherwise directed on the label.

Use In Special Populations

Elderly: No dose adjustment is required for Tearon 0.4%+0.3% in elderly patients; dry eye is common in this population and Tearon 0.4%+0.3% may be used as needed.

Renal/Hepatic impairment: Not applicable, as Tearon 0.4%+0.3% is a topical ophthalmic product with minimal systemic absorption.

Contact lens wearers: Remove contact lenses before use unless the specific formulation is labeled safe for use with lenses in place.

Duration Of Treatment

Tearon 0.4%+0.3% may be used as needed for symptomatic relief of dry eye. For chronic or persistent dry eye symptoms lasting more than 72 hours despite regular use, or if symptoms worsen, discontinue use and consult a physician to evaluate for an underlying cause.

Drug Classes

Ophthalmic lubricants / artificial tears (drugs for dry eyes)

Mode Of Action

Tearon 0.4%+0.3% acts as a demulcent and lubricant on the ocular surface. Polyethylene glycol 400 and propylene glycol increase the viscosity and water-retention of the tear film, coating the cornea and conjunctiva to reduce friction, stabilize the pre-corneal tear film, and provide symptomatic relief from dryness and irritation.

Pediatric Uses

Safety and efficacy of Tearon 0.4%+0.3% in pediatric patients have not been formally established in controlled trials; however, as an over-the-counter topical ophthalmic lubricant with minimal systemic absorption, it is commonly used in children under caregiver supervision for symptomatic dry eye relief. Use in infants and young children should be under the guidance of a physician.

Frequently Asked Questions

Q: What is Tearon 0.4%+0.3% used for?

A: Tearon 0.4%+0.3% is an ophthalmic lubricant (artificial tears) used for the temporary relief of burning, irritation, and discomfort caused by dryness of the eye.

Q: How often can I use Tearon 0.4%+0.3% eye drops?

A: Typically, 1 to 2 drops of Tearon 0.4%+0.3% can be instilled in the affected eye(s) as needed, up to 4 times daily, or as directed by your physician.

Q: Can I use Tearon 0.4%+0.3% while wearing contact lenses?

A: Contact lenses should generally be removed before instilling Tearon 0.4%+0.3% unless your specific product is labeled as safe for use with lenses in place. Check the product label or ask your pharmacist or physician.

Q: Is Tearon 0.4%+0.3% safe during pregnancy and breastfeeding?

A: There are no well-controlled studies of Tearon 0.4%+0.3% in pregnancy or lactation, but as a topical eye product with minimal systemic absorption, significant risk is not expected. It should still be used only if clearly needed, and you should consult a physician or pharmacist before use.

Q: What should I do if my eye pain or redness does not improve?

A: If you experience eye pain, vision changes, or redness/irritation that persists beyond 72 hours or worsens while using Tearon 0.4%+0.3%, stop use and seek medical evaluation, as this may indicate a condition requiring specific treatment.

Q: What if I accidentally swallow Tearon 0.4%+0.3%?

A: Tearon 0.4%+0.3% is intended for eye use only. If accidentally swallowed and symptoms occur, or a large amount is ingested, seek immediate medical attention or contact a poison control center.

Disclaimer

The information provided is accurate to the best of our knowledge, but it does not replace professional medical advice. We cannot guarantee its completeness or accuracy, and the absence of specific information about a drug should not be taken as an endorsement. We are not responsible for any consequences arising from this information, so please consult a healthcare professional for any concerns or questions.

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