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.
From the official U.S. FDA label for potassium iodide, the active ingredient registered with NAFDAC.
For temporary relief of discomfort associated with lymphatic swelling and edema. Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Purpose "X" indicates a homeopathic dilution. For more information visit: www.hevertusa.com Arsenicum album 6X Relief of discomfort associated with lymphatic swelling and edema Clematis 4X Conium 6X L …
you suffer from thyroid disease or symptoms persist for more than 7 days, worsen or new symptoms occur.
if you are allergic to Rhus toxicodendron or other plants from the cashew family
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. …
If pregnant or breast-feeding, ask a health professional before use.
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.
Add the expiry date on your pack for a full Trust Score.
Catarest Eye Drop contains Potassium iodide; Sodium chloride; Calcium chloride (3.3%; 0.83%; 1%), as solution/drops, according to its NAFDAC registration record.
Yes. Catarest Eye Drop is listed on the NAFDAC register under registration number A4-5725, and its registration is active as of 28 October 2026.
No WHO falsified or substandard medical product alert currently matches Catarest Eye Drop in our automatically synced alert list.
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.
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. Always follow your doctor or pharmacist.)
Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.