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 sodium hyaluronate, the active ingredient registered with NAFDAC.
instantly helps relieveanorectal itching and discom-fort such as pain, soreness, orburning commonly associatedwith hemorrhoids temporarily protects theinflamed, irritated anorectalarea to make future bowelmovements less painful fromirritation and abrasion
Adsorbent and detoxifying Healing and barrier protection Hydration and wound healing Humectant and moisturizing
For external use.
STAY FRESH,COMFORTABLE,AND CLEAN.
Add the expiry date printed on your pack for a full Trust Score — or look up uses, side effects and cheaper generics.
Hyorth XL Injection## (strength format) contains Sodium Hyaluronate; DI Sodium Hydrogen Phosphate Dihydrate; Monosodium Phosphate Monohydrate; Sodium Chloride (8mg; 0.16mg; 0.04mg; 8.5mg), as injection, according to its NAFDAC registration record.
Yes. Hyorth XL Injection## (strength format) is listed on the NAFDAC register under registration number B4-7863, and its registration is active as of 5 November 2026.
No WHO falsified or substandard medical product alert currently matches Hyorth XL Injection## (strength format) in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number B4-7863, 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.
instantly helps relieveanorectal itching and discom-fort such as pain, soreness, orburning commonly associatedwith hemorrhoids temporarily protects theinflamed, irritated anorectalarea to make future bowelmovements less painful fromirritation and abrasion (Summarised from the official U.S. FDA label for sodium hyaluronate. 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.