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Accueil / Enregistré au Nigeria / Acretin 0.025% Cream

Acretin 0.025% Cream

NAFDAC REG NO: B4-7657 Médicament

Enregistré auprès de NAFDAC. Enregistrement actifAs of 5 November 2026 · synced automatically from official sources.
Produit
Acretin 0.025% Cream
Numéro NAFDAC
B4-7657
Principe actif
Tretinoin
Dosage
0.025%
Forme
Crème
Conditionnement
1 x 30 g (in Aluminum tube)
Fabricant
Non répertorié
Déposant / Titulaire :
Assene-Laborex Limited
Approuvé
27 Jun 2024
Statut
Actif Vue sur NAFDAC ↗
Enregistrement valable jusqu'au
26 Jun 2029
Alertes OMS
Non trouvé
Community reports
None
Times checked
0

About the medicine: Tretinoin: uses, dosage and brands worldwide

What we found

  • Acretin 0.025% Cream is on the NAFDAC register with an active registration (B4-7657). 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 Acretin 0.025% Cream

Ce que dit la notice officielle. Si un médecin vous l'a prescrit, suivez l'ordonnance. La notice de votre boîte prime si elle est différente.

Mise en garde grave : EMBRYO-FETAL TOXICITY and DIFFERENTIATION SYNDROME • Tretinoin capsules can cause embryo-fetal loss and malformations when administered to a pregnant woman. Advise pregnant women of the potential risk to a fetus. Females of reproductive potential must have a negative pregnancy test before initiating tretinoin capsules. Advise females of reproductive potential to use two effective methods of contraception during treatment with tretinoin capsules and for 1 month after the last dose. …
Pour qui

Tretinoin capsules are indicated for the induction of remission in adults and pediatric patients 1 year of age and older with acute promyelocytic leukemia (APL) characterized by the presence of the t(15;17) translocation or PML/RARα gene expression, and who are refractory to or who have relapsed from anthracycline chemotherapy or for whom anthracycline-based chemotherapy is contraindicated. …

Comment le prendre et à quelle fréquence
  • The recommended dosage of tretinoin capsules is 22.5 mg/m 2 orally twice daily until complete remission. • Discontinue 30 days after achievement of complete remission or after 90 days of treatment, whichever occurs first
  • Important Safety Information Verify pregnancy status in females of reproductive potential prior to initiating tretinoin capsules
  • Females of reproductive potential must have a negative pregnancy test before initiating tretinoin capsules [see Use in Specific Populations ]
  • Recommended Dosage The recommended dosage of tretinoin capsules is 22.5 mg/m 2 orally twice daily until complete remission is documented
  • Discontinue tretinoin capsules 30 days after achievement of complete remission or after 90 days of treatment, whichever occurs first
  • Discontinue tretinoin capsules if the t(15;17) translocation or PML/RARα fusion has not been identified [see Warnings and Precautions ]
  • Take tretinoin capsules with a meal
  • Swallow tretinoin capsules whole with water
  • Do not chew, dissolve, or open capsule
  • Do not take a missed dose of tretinoin capsules unless it is more than 10 hours until the next scheduled dose
  • If vomiting occurs after tretinoin capsules administration, do not take an additional dose, but continue with the next scheduled dose
  • Important Safety Information Verify pregnancy status in females of reproductive potential prior to initiating tretinoin capsules
  • Females of reproductive potential must have a negative pregnancy test before initiating tretinoin capsules [see Use in Specific Populations ] . …
Strengths it comes in

Capsules: 10 mg, two-tone (lengthwise) with reddish-brown opaque and yellow gelatin shell, imprinted with “TR” with black ink on the yellow side. Capsules: 10 mg ( 3 )

Children
  • Safety and effectiveness of tretinoin capsules have been established
  • In pediatric patients 1 year of age and older and the information on this use is discussed throughout the labeling
  • The maximum tolerated dose is lower
  • In pediatric patients compared to adults
  • Some
  • Pediatric patients experience severe headache and intracranial hypertension, which required management with an analgesic and a lumbar puncture
  • Dose reduction may be considered for pediatric patients experiencing serious and/or intolerable adverse reactions. …
Older adults

Across clinical studies of tretinoin capsules, 21% were 60 years and older. No overall differences in safety or effectiveness were observed between these patients and younger patients.

While you are taking it
  • Embryo-Fetal Toxicity Advise female patients of the potential risk to a fetus
  • Advise females of reproductive potential to inform their healthcare provider of a known or suspected pregnancy [see Warnings and Precautions and Use in Specific Populations ]
  • Advise females of reproductive potential to use 2 methods of effective contraception during treatment with tretinoin capsules and for 1 month after the last dose [see Use in Specific Populations ]
  • Advise males with female partners of reproductive potential to use effective contraception during treatment with tretinoin capsules and for 1 week after the last dose [see Use in Specific Populations ] . …
Talk to a doctor first if
  • Tretinoin capsules are contraindicated in patients with a known hypersensitivity to tretinoin capsules, any of its components, or other retinoids
  • Reactions have included rash, pruritus, face edema, and dyspnea [see Adverse Reactions ]
  • Hypersensitivity to tretinoin capsules, any of its components, or other retinoids
Medicines it may not mix with

• Strong CYP3A Inhibitors and Inducers: Avoid coadministration with strong CYP3A inhibitors and inducers. ( 7.1 ) • Concomitant Use of Products Known to Cause Intracranial Hypertension : Avoid concomitant use with other products that can cause intracranial hypertension. ( 7.2 ) • Vitamin A : Avoid concomitant use with vitamin A. ( 7.3 ) • Anti-fibrinolytic Agents : Avoid concomitant use with anti-fibrinolytic agents. ( 7.4 ) 7.1 Effects of Other Drugs on Tretinoin Capsules Strong or moderate CYP3A Inhibitors Avoid concomitant use of tretinoin capsules with strong CYP3A inhibitors if possible and monitor more frequently if concomitant use is unavoidable. …

Warnings

• Patients Without t(15;17) Translocation or PML/RARα Fusion: Tretinoin capsules may be initiated based on morphological diagnosis of APL. Confirm diagnosis by detection of the t(15;17) translocation or PML/RARα fusion. ( 5.3 ) • Leukocytosis: Consider administering cytoreductive chemotherapy (including an anthracycline if not contraindicated or hydroxyurea) with tretinoin capsules in the setting of leukocytosis, as clinically indicated. ( 5.4 ) • Intracranial Hypertension: Tretinoin capsules have been associated with benign intracranial hypertension, especially in pediatric patients. Consider interruption, dose reduction, or discontinuation of tretinoin capsules as appropriate. …

Effets secondaires possibles

The following clinically significant adverse reactions are described elsewhere in the labeling: • Differentiation Syndrome [see Warnings and Precautions ( 5.2 )] • Leukocytosis [see Warnings and Precautions ( 5.4 )] • Intracranial hypertension [see Warnings and Precautions (5.5)] • Lipid abnormalities [see Warnings and Precautions ( 5.6 )] • Hepatotoxicity [see Warnings and Precautions ( 5.7 )] • Thromboembolic events [see Warnings and Precautions (5 .8 )] The most common adverse reactions (≥30%) are headache, fever, skin/mucous membrane dryness, bone pain, malaise, shivering, upper respiratory tract disorders, dyspnea, hemorrhage, infections, nausea/vomiting, rash, peripheral edema, leukocy …

Pregnancy and breastfeeding

8.1 Pregnancy Risk Summary Based on findings in animals and its mechanism of action [see Clinical Pharmacology ( 12.1 )], tretinoin capsules can cause embryo-fetal loss and malformations when administered to a pregnant woman. Tretinoin capsules are a retinoid and there is an increased risk of major congenital malformations, spontaneous abortions and premature births following exposure to retinoids during pregnancy in humans. …

If you take too much

In case of overdose with tretinoin capsules, reversible signs of hypervitaminosis A (headache, nausea, vomiting, mucocutaneous symptoms) can appear. Overdosage with other retinoids has been associated with transient headache, facial flushing, cheilosis, abdominal pain, dizziness and ataxia. These symptoms have quickly resolved without apparent residual effects. There is no specific treatment in the case of an overdose; however, it is important that the patient be treated in a special hematological unit.

En cas d'oubli

Prenez-le dès que vous y pensez, sauf s'il est presque l'heure de la dose suivante. Dans ce cas, sautez la dose oubliée. Ne prenez jamais deux doses à la fois pour compenser. Vérifiez votre notice, certains médicaments font exception.

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 2026-05-26.

Label for tretinoin, the active ingredient registered with NAFDAC.

Check your pack of Acretin 0.025% Cream

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

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About Acretin 0.025% Cream

What is in Acretin 0.025% Cream?

Acretin 0.025% Cream contains Tretinoin (0.025%), as cream, according to its NAFDAC registration record.

Is Acretin 0.025% Cream registered with NAFDAC?

Yes. Acretin 0.025% Cream is listed on the NAFDAC register under registration number B4-7657, and its registration is active as of 5 November 2026.

Has Acretin 0.025% Cream been flagged as fake or recalled?

No WHO falsified or substandard medical product alert currently matches Acretin 0.025% Cream in our automatically synced alert list.

How can I check that my pack of Acretin 0.025% Cream is genuine?

Run a free authenticity scan with the NAFDAC number B4-7657, 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 Acretin 0.025% Cream?

Follow your prescription or the leaflet in your pack. The official label says: • The recommended dosage of tretinoin capsules is 22.5 mg/m 2 orally twice daily until complete remission. ( 2.2 ) • Discontinue 30 days after achievement of complete remission or after 90 days of treatment, whichever occurs first. ( 2.2 ) 2.1 Important Safety Information Verify pregnancy status in females of reproductive potential prior to initiating tretinoin capsules. Female…

What is Acretin 0.025% Cream used for?

Tretinoin capsules are indicated for the induction of remission in adults and pediatric patients 1 year of age and older with acute promyelocytic leukemia (APL) characterized by the presence of the t(15;17) translocation or PML/RARα gene expression, and who are refractory to or who have relapsed from anthracycline chemotherapy or for whom anthracycline-based chemotherapy is contraindicated. … (Summarised from the official U.S. FDA label for tretinoin. Always follow your doctor or pharmacist.)

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