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Openna Eye Drops

NAFDAC Reg.-Nr. B4-3702 Medikament

Registriert bei NAFDAC. Registrierung aktivAs of 29 October 2026 · synced automatically from official sources.
Produkt-
Openna Eye Drops
NAFDAC-Nummer
B4-3702
Wirkstoff
Cyclopentolate Hydrochloride
Stärke
1%
Form
Solution/Drops
VPE:
1 x 10 mL (in bottle)
Hersteller
Not listed
Applicant (holder)
Lin-Kabs Pharmaceutical Limited
Approved
28 Oct 2021
Status
Inactive View on NAFDAC ↗
Registration valid to
27 Oct 2026
WER WARNT
None found
Community reports
None
Times checked
0

What we found

  • Openna Eye Drops is on the NAFDAC register with an active registration (B4-3702). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

Generated automatically from the NAFDAC register, WHO alerts and community data as of today. This is not medical advice. Always follow your doctor or pharmacist.

How to use Openna Eye Drops

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

Cyclopentolate hydrochloride is used to produce mydriasis and cycloplegia.

How to take it and how often
  • Adults: Instill one or two drops of 0.5%, 1% or 2% solution in the eye which may be repeated in five to ten minutes if necessary
  • Complete recovery usually occurs in 24 hours
  • Complete recovery from mydriasis in some individuals may require several days
  • Children: Instill one or two drops of 0.5%, 1% or 2% solution in the eye which may be repeated five to ten minutes later by a second application of 0.5% or 1% solution if necessary
  • Small
  • Infants: A single instillation of one drop of 0.5% in the eye
  • To minimize absorption, apply pressure over the nasolacrimal sac for two to three minutes
  • Observe infant closely for at least 30 minutes following instillation
  • Individuals with heavily pigmented irides may require higher strengths
Children
  • Use of cyclopentolate has been associated with psychotic reactions and behavioral disturbances
  • In pediatric patients
  • Increased susceptibility to cyclopentolate has been reported in infants, young children, and in children with spastic paralysis or brain damage
  • These disturbances include ataxia, incoherent speech, restlessness, hallucinations, hyperactivity, seizures, disorientation as to time and place, and failure to recognize people
  • Feeding intolerance and necrotizing enterocolitis (NEC) in preterm
  • Infants may follow ophthalmic use of this product. …
Older adults

No overall differences in safety or effectiveness have been observed between elderly and younger patients.

While you are taking it
  • Do not touch dropper tip to any surface, as this may contaminate the solution
  • A transient burning sensation may occur upon instillation
  • Patients should be advised not to drive or engage in other hazardous activities while pupils are dilated
  • Patients may experience sensitivity to light and should protect eyes in bright illumination during dilation
  • Parents should be warned not to get this preparation in their child's mouth and to wash their own hands and the child's hands following administration
  • Feeding intolerance may follow ophthalmic use of this product in infants
  • It is recommended that feeding be withheld for 4 hours after examination
Talk to a doctor first if

Should not be used if the patient is hypersensitive to any component of this preparation.

Medicines it may not mix with

Cyclopentolate may interfere with the ocular anti-hypertensive action of carbachol, pilocarpine, or ophthalmic cholinesterase inhibitors.

Warnings

FOR TOPICAL OPHTHALMIC USE ONLY . NOT FOR INJECTION. This preparation may cause Central Nervous System (CNS) disturbances. This is especially true in younger age groups, but may occur at any age, especially with the stronger solutions. Infants are especially prone to CNS and cardiopulmonary side effects from cyclopentolate. To minimize absorption, use only 1 drop of 0.5% CYCLOGYL solution per eye, followed by pressure applied over the nasolacrimal sac for two to three minutes. Observe infants closely for at least 30 minutes following instillation. Mydriatics may produce a transient elevation of intraocular pressure. …

Possible side effects

Ocular: Increased intraocular pressure, burning, photophobia, blurred vision, irritation, hyperemia, conjunctivitis, blepharoconjunctivitis, punctate keratitis, synechiae have been reported. Non-ocular: Use of cyclopentolate has been associated with psychotic reactions and behavioral disturbances, usually in children, especially with 2% concentration. These disturbances include ataxia, incoherent speech, restlessness, hallucinations, hyperactivity, seizures, disorientation as to time and place, and failure to recognize people. This drug produces reactions similar to those of other anticholinergic drugs, but the central nervous system manifestations as noted above are more common. …

Pregnancy and breastfeeding

Pregnancy: Animal reproduction studies have not been conducted with cyclopentolate. It is also not known whether cyclopentolate can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Cyclopentolate should be administered to a pregnant woman only if clearly needed.

If you take too much

Excessive dosage may produce behavioral disturbances, tachycardia, hyperpyrexia, hypertension, elevated intraocular pressure, vasodilation, urinary retention, diminished gastrointestinal motility and decreased secretion in salivary and sweat glands, pharynx, bronchi and nasal passages. Patients exhibiting signs of overdosage should receive supportive care and monitoring.

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2024-06-25.

Label for cyclopentolate hydrochloride, the active ingredient registered with NAFDAC.

Check your pack of Openna Eye Drops

Add the expiry date on your pack for a full Trust Score.

Or take photos of the pack
3 free checks left today Official sources: U.S. FDA · EMA (EU) · NAFDAC · WHO alerts

About Openna Eye Drops

What is in Openna Eye Drops?

Openna Eye Drops contains Cyclopentolate Hydrochloride (1%), as solution/drops, according to its NAFDAC registration record.

Is Openna Eye Drops registered with NAFDAC?

Yes. Openna Eye Drops is listed on the NAFDAC register under registration number B4-3702, and its registration is active as of 29 October 2026.

Has Openna Eye Drops been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Openna Eye Drops in our automatically synced alert list.

How can I check that my pack of Openna Eye Drops is genuine?

Run a free authenticity scan with the NAFDAC number B4-3702, your pack's expiry date and batch number to get a Trust Score, compare the pack with the NAFDAC record (ingredient, strength, form, manufacturer), and buy only from licensed pharmacies.

How do I take Openna Eye Drops?

Follow your prescription or the leaflet in your pack. The official label says: Adults: Instill one or two drops of 0.5%, 1% or 2% solution in the eye which may be repeated in five to ten minutes if necessary. Complete recovery usually occurs in 24 hours. Complete recovery from mydriasis in some individuals may require several days. Children: Instill one or two drops of 0.5%, 1% or 2% solution in the eye which may be repeated five to ten minutes later by a…

What is Openna Eye Drops used for?

Cyclopentolate hydrochloride is used to produce mydriasis and cycloplegia. (Summarised from the official U.S. FDA label for cyclopentolate hydrochloride. Always follow your doctor or pharmacist.)

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