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 diclofenac sodium, the active ingredient registered with NAFDAC.
(s) for the temporary relief of arthritis pain ONLY in the following areas head, wrist, elbow (upper body areas) foot, ankle, knee (lower body areas) this product may take up to 7 days to work for arthritis pain; it is not for immediate relief. If no pain relief in 7 days, stop use.
Arthritis pain reliever
pain gets worse or lasts more than 21 days redness or swelling is present in the painful area fever occurs skin irritation occurs any new symptoms appear. These could be signs of a serious condition. you experience any of the following signs of stomach bleeding: feel faint have bloody or black stools vomit blood have stomach pain that does not get better you have symptoms of heart problems or stroke: chest pain trouble breathing leg swelling weakness in one part of side of body slurred speech
if you have ever had an allergic reaction to any other pain reliever or to a fever reducer for strains, sprains, bruises or sports injuries. This product has not been shown to work for these types of injuries. right before or after heart surgery on more than 2 body areas at the same time in the eyes, nose or mouth
For external use only Allergy alert: Diclofenac may cause a severe allergic reacction, expecially in people allergic to aspirin. Symptoms may include: hives asthma (wheezing) skin reddening blisters facial swelling shock rash If an allergic reaction occurs, stop use and seek medical help right away. Liver warning: This product contains diclofenac. Liver damage may occur if you apply: more or for a longer time than directed when using other drugs containing diclofenac Stomach bleeding warning: This product contains an NSAID, which may cause severe stomach bleeding. …
Pregnancy/Breastfeeding If pregnant or breast-feeding, ask a health professional before use. It is especially important not to use diclofenac at 20 weeks or later in pregnancy unless definitely directed to do so by a doctor because it may cause problems in the unborn child or complications during delivery.
Storage store at 20˚ to 25˚C (68˚ to 77˚F). Keep from freezing.
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Derm Diclofenac Injection Diclofenac Sodium contains Diclofenac Sodium (75 mg/3 mL), as injection, according to its NAFDAC registration record.
Yes. Derm Diclofenac Injection Diclofenac Sodium is listed on the NAFDAC register under registration number A4-6898, and its registration is active as of 6 November 2026.
No WHO falsified or substandard medical product alert currently matches Derm Diclofenac Injection Diclofenac Sodium in our automatically synced alert list.
Run a free authenticity scan with the NAFDAC number A4-6898, 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.
(s) for the temporary relief of arthritis pain ONLY in the following areas head, wrist, elbow (upper body areas) foot, ankle, knee (lower body areas) this product may take up to 7 days to work for arthritis pain; it is not for immediate relief. If no pain relief in 7 days, stop use. (Summarised from the official U.S. FDA label for diclofenac sodium. 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.