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Curegold 4 mg Tablet

NAFDAC Reg. No. A4-8554 · Drug

Registered with NAFDAC. Registration activeAs of 28 October 2026 · synced automatically from official sources.
Product
Curegold 4 mg Tablet
NAFDAC number
A4-8554
Active ingredient
Cyproheptadine Hydrochloride
Strength
4 mg
Form
Tablet
Pack size
3 x 10's (in PVC/PVDC blister foil and aluminium foil)
Manufacturer
Not listed
Applicant (holder)
Unicure Pharmaceuticals Limited
Approved
28 Aug 2024
Status
Active View on NAFDAC ↗
Registration valid to
27 Aug 2029
WHO alerts
None found
Community reports
None
Times checked
0

What we found

  • Curegold 4 mg Tablet is on the NAFDAC register with an active registration (A4-8554). A valid number alone does not prove a pack is genuine — counterfeiters copy real numbers, so also check the expiry date, seal and print quality.

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.

How to use Curegold 4 mg Tablet

What the official label says. If a doctor prescribed it, follow the prescription. Your pack's leaflet comes first if it is different.

Who it is for

Perennial and seasonal allergic rhinitis, Vasomotor rhinitis, Allergic conjunctivitis due to inhalant allergens and foods. Mild, uncomplicated allergic skin manifestations of urticaria and angioedema. Amelioration of allergic reactions to blood or plasma. Cold urticaria. Dermatographism. As therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute manifestations have been controlled.

How to take it and how often
  • DOSAGE SHOULD BE INDIVIDUALIZED ACCORDING TO THE NEEDS AND THE RESPONSE OF THE PATIENT
  • Children: The total daily dosage for children may be calculated on the basis of body weight or body area using approximately 0.25 mg/kg/day (0.11 mg/lb/day) or 8 mg per square meter of body surface (8 mg/m 2 )
  • In small children for whom the calculation of the dosage based upon body size is important, it may be necessary to use cyproheptadine syrup to permit accurate dosage
  • Age 2 to 6 years: The usual dose is 2 mg (1/2 tablet) two or three times a day, adjusted as necessary to the size and response of the patient
  • The dose is not to exceed 12 mg a day
  • Age 7 to 14 years: The usual dose is 4 mg (1 tablet) two or three times a day, adjusted as necessary to the size and response of the patient
  • The dose is not to exceed 16 mg a day
  • Adults: The total daily dose for
  • Adults should not exceed 0.5 mg/kg/day (0.23 mg/lb/day)
  • The therapeutic range is 4 to 20 mg a day, with the majority of patients requiring 12 to 16 mg, a day
  • An occasional patient may require as much as 32 mg a day for adequate relief
  • It is suggested that dosage be initiated with 4 mg (1 tablet) three times a day and adjusted according to the size and response of the patient
Talk to a doctor first if
  • Newborn or Premature
  • Infants: This drug should not be used in newborn or premature
  • Infants
  • Nursing Mothers: Because of the higher risk of antihistamines for
  • Infants generally, and for newborns and prematures in particular, antihistamine therapy is contraindicated in nursing mothers
  • Other Conditions: Hypersensitivity to cyproheptadine and other drugs of similar chemical structure
  • Monoamine oxidase inhibitor therapy (see DRUG INTERACTIONS )
  • Angle-closure glaucoma
  • Stenosing peptic ulcer. …
Warnings

Children - Overdosage of antihistamines, particularly in infants and children, may produce hallucinations, central nervous system depression, convulsions, and death. Antihistamines may diminish mental alertness conversely particularly in the young child they may occasionally produce excitation. CNS Depressants - Antihistamines may have additive effects with alcohol and other CNS depressants, e.g., hypnotics, sedatives, tranquilizers, antianxiety agents. Activities Requiring Mental Alertness - Patients should be warned about engaging in activities requiring mental alertness and motor coordination, such as driving a car or operating machinery. …

Possible side effects

Adverse reactions which have been reported with the use of antihistamines are as follows: Central Nervous System: Sedation and sleepiness (often transient), dizziness, disturbed coordination, confusion, restlessness, excitation, nervousness, tremor, irritability, insomnia, paresthesias, neuritis, convulsions, euphoria, hallucinations, hysteria, faintness. Integumentary: Allergic manifestation of rash and edema, excessive perspiration, urticaria, photosensitivity. Special Senses: Acute labyrinthitis, blurred vision, diplopia, vertigo, tinnitus. Cardiovascular: Hypotension, palpitation, tachycardia, extrasystoles, anaphylactic shock. …

Pregnancy and breastfeeding

PREGNANCY Pregnancy Category B: Reproduction studies have been performed in rabbits, mice, and rats at oral or subcutaneous doses up to 32 times the maximum recommended human oral dose and have revealed no evidence of impaired fertility or harm to the fetus due to cyproheptadine. Cyproheptadine has been shown to be fetotoxic in rats when given by intraperitoneal injection in doses four times the maximum recommended human oral dose. …

If you take too much

Antihistamine overdosage reactions may vary from central nervous system depression to stimulation, especially in children. Also, atropine-like signs and symptoms (dry mouth; fixed, dilated pupils; flushing, etc.) as well as gastrointestinal symptoms may occur. If vomiting has not occurred spontaneously, the patient should be induced to vomit with syrup of ipecac. If patient is unable to vomit, perform gastric lavage followed by activated charcoal. Isotonic or 1/2 isotonic saline is the lavage of choice. Precautions against aspiration must be taken, especially in infants and children. …

If you miss a dose

Take it when you remember, unless it is nearly time for the next dose. Then skip the missed one. Never take two doses at once to make up for it. Check your leaflet, as some medicines are different.

From the official U.S. FDA label for this active ingredient. Your pack may have a different strength, so always read its leaflet. If a doctor prescribed it, follow the prescription. Ask a pharmacist if you are unsure. Label dated 2023-01-27.

Label for cyproheptadine hydrochloride, the active ingredient registered with NAFDAC.

Check your pack of Curegold 4 mg Tablet

Add the expiry date on your pack for a full Trust Score.

3 free checks left today Official sources: NAFDAC · WHO · U.S. FDA · Health Canada · NLM

About Curegold 4 mg Tablet

What is in Curegold 4 mg Tablet?

Curegold 4 mg Tablet contains Cyproheptadine Hydrochloride (4 mg), as tablet, according to its NAFDAC registration record.

Is Curegold 4 mg Tablet registered with NAFDAC?

Yes. Curegold 4 mg Tablet is listed on the NAFDAC register under registration number A4-8554, and its registration is active as of 28 October 2026.

Has Curegold 4 mg Tablet been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Curegold 4 mg Tablet in our automatically synced alert list.

How can I check that my pack of Curegold 4 mg Tablet is genuine?

Run a free authenticity scan with the NAFDAC number A4-8554, 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.

How do I take Curegold 4 mg Tablet?

Follow your prescription or the leaflet in your pack. The official label says: DOSAGE SHOULD BE INDIVIDUALIZED ACCORDING TO THE NEEDS AND THE RESPONSE OF THE PATIENT. Children: The total daily dosage for children may be calculated on the basis of body weight or body area using approximately 0.25 mg/kg/day (0.11 mg/lb/day) or 8 mg per square meter of body surface (8 mg/m 2 ). In small children for whom the calculation of the dosage based upon body size is …

What is Curegold 4 mg Tablet used for?

Perennial and seasonal allergic rhinitis, Vasomotor rhinitis, Allergic conjunctivitis due to inhalant allergens and foods. Mild, uncomplicated allergic skin manifestations of urticaria and angioedema. Amelioration of allergic reactions to blood or plasma. Cold urticaria. Dermatographism. As therapy for anaphylactic reactions adjunctive to epinephrine and other standard measures after the acute man (Summarised from the official U.S. FDA label for cyproheptadine hydrochloride. Always follow your doctor or pharmacist.)

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Reviews are personal experiences from PillVera users, not medical advice. Report side effects to your doctor and to NAFDAC.