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Catarest Eye Drop

NAFDAC Reg. No. A4-5725 · Drug

Registered with NAFDAC. Registration activeAs of 5 November 2026 · synced automatically from official sources.
Product
Catarest Eye Drop
Número NAFDAC
A4-5725
Princípio ativo
Potassium iodide; Sodium chloride; Calcium chloride
Dosagem
3.3%; 0.83%; 1%
Forma
Solution/Drops
Tamanho da embalagem
10 mL (in Lupolen vial)
Manufacturer
Not listed
Applicant (holder)
Al-Tinez Pharmaceuticals Limited
Approved
7 May 2021
Situação
Inactive View on NAFDAC ↗
Registro válido até
6 Mar 2026
Alertas da OMS
None found
Community reports
None
Times checked
0

About the medicine: Potassium iodide: uses, dosage and brands worldwide

What we found

  • Catarest Eye Drop is on the NAFDAC register with an active registration (A4-5725). 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 Catarest Eye Drop

O que diz a bula oficial. Se um médico receitou, siga a receita. Se a bula da sua caixa for diferente, vale a da sua caixa.

Para quem é

For temporary relief of discomfort associated with lymphatic swelling and edema. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Como tomar e com que frequência
  • Adults and children over 12 years of age: Take 20 drops in water 3 times daily
  • Consult a physician for use in children under 12 years of age
  • Do not use for children under 1 year of age
Talk to a doctor first if
  • Chronically enlarged lymph nodes can be the sign of different diseases
  • Therefore, consult a doctor in order to clarify the underlying disease before using this medicine
  • Also consult a doctor promptly in case of acute signs of inflammation (redness, heat, swelling, pain and dysfunction) and fever or enlargement of the lymph nodes during treatment
Warnings

For oral use only. Chronically enlarged lymph nodes can be the sign of different diseases. Therefore, consult a doctor in order to clarify the underlying disease before using this medicine. Also consult a doctor promptly in case of acute signs of inflammation (redness, heat, swelling, pain and dysfunction) and fever or enlargement of the lymph nodes during treatment. Do not use if you are allergic to Rhus toxicodendron or other plants from the cashew family Stop use and ask a doctor if you suffer from thyroid disease or symptoms persist for more than 7 days, worsen or new symptoms occur. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. …

Possíveis efeitos colaterais

You suffer from thyroid disease or symptoms persist for more than 7 days, worsen or new symptoms occur.

Pregnancy and breastfeeding

If pregnant or breast-feeding, ask a health professional before use.

How to store it

Store at 68 to 77 °F. Tamper Evident: Do not use if tamper evident strip is broken or missing from base of bottle cap. To report serious adverse events, call 1-855-387-6466. Keep out of reach of children.

Se esquecer uma dose

Tome assim que lembrar, a menos que esteja quase na hora da próxima dose. Nesse caso, pule a dose esquecida. Nunca tome duas doses de uma vez para compensar. Confira a bula, pois alguns medicamentos são diferentes.

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 2022-12-20.

Label for potassium iodide and sodium chloride and calcium chloride, the active ingredient registered with NAFDAC.

Check your pack of Catarest Eye Drop

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

Ou tire fotos da caixa
Restam 3 verificações grátis hoje Official sources: U.S. FDA · EMA (EU) · Health Canada · WHO alerts

About Catarest Eye Drop

What is in Catarest Eye Drop?

Catarest Eye Drop contains Potassium iodide; Sodium chloride; Calcium chloride (3.3%; 0.83%; 1%), as solution/drops, according to its NAFDAC registration record.

Is Catarest Eye Drop registered with NAFDAC?

Yes. Catarest Eye Drop is listed on the NAFDAC register under registration number A4-5725, and its registration is active as of 5 November 2026.

Has Catarest Eye Drop been flagged as fake or recalled?

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

How can I check that my pack of Catarest Eye Drop is genuine?

Run a free authenticity scan with the NAFDAC number A4-5725, 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 Catarest Eye Drop?

Follow your prescription or the leaflet in your pack. The official label says: Adults and children over 12 years of age: Take 20 drops in water 3 times daily. Consult a physician for use in children under 12 years of age. Do not use for children under 1 year of age.…

What is Catarest Eye Drop used for?

For temporary relief of discomfort associated with lymphatic swelling and edema. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. (Summarised from the official U.S. FDA label for potassium iodide and sodium chloride and calcium chloride. Always follow your doctor or pharmacist.)

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Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.