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 insulin regular (human), the active ingredient registered with NAFDAC.
INDICATIONS For the temporary relief of general weakness, debilitation, excessive sweating, or minor skin rash or hives due to sensitivity to phenolic compounds found in foods or other products.*
*Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
In case of overdose, get medical help or contact a poison control center right away. Keep out of the reach of children. If pregnant or breastfeeding, ask a healthcare professional before use.
If pregnant or breastfeeding, ask a healthcare professional before use.
Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.
Humulin R Solution for Injection in Cartridge contains Insulin regular (Human) (300 units/3 mL), as solution for injection, according to its NAFDAC registration record.
Yes. Humulin R Solution for Injection in Cartridge is listed on the NAFDAC register under registration number A6-0271, and its registration is active as of 6 November 2026.
No WHO falsified or substandard medical product alert currently matches Humulin R Solution for Injection in Cartridge in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number A6-0271, 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.
INDICATIONS For the temporary relief of general weakness, debilitation, excessive sweating, or minor skin rash or hives due to sensitivity to phenolic compounds found in foods or other products.* (Summarised from the official U.S. FDA label for insulin regular (human). 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.