Generated automatically from the NAFDAC register, WHO alerts and community data as of today. Not medical advice — always follow your doctor or pharmacist.
From the official U.S. FDA label for potassium chloride, the active ingredient registered with NAFDAC.
For handwashing to decrease bacteria on the skin
Antibacterial
irritation and redness develop condition persists for more than 72 hours
For external use only: hands only
Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.
Srowk Tablets Prolonged Release Potassium Chloride contains Potassium chloride (600 mg), as prolonged-release tablet, according to its NAFDAC registration record.
Yes. Srowk Tablets Prolonged Release Potassium Chloride is listed on the NAFDAC register under registration number A4-101103, and its registration is active as of 6 November 2026.
No WHO falsified or substandard medical product alert currently matches Srowk Tablets Prolonged Release Potassium Chloride in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number A4-101103, 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 handwashing to decrease bacteria on the skin (Summarised from the official U.S. FDA label for potassium chloride. Always follow your doctor or pharmacist.)
Reviews are personal experiences from RxVerify users, not medical advice. Report side effects to your doctor and to NAFDAC.