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Connect with Your Dermatology Provider from the Comfort of Your Home.

Due to the outbreak of COVID-19, it’s now possible to connect virtually for examinations, recommendations, along with having prescriptions filled to treat your facial melasma. Contact your dermatology provider to find out if voice or video conferencing is now being offered.

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Prescribing Information

TriLuma

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  • About Tri-Luma® Cream
    • About
    • How to Use
    • Safety & Side Effects
    • Frequently Asked Questions
  • Melasma Check Test
  • About Melasma
    • What is melasma?
    • Who gets melasma?
    • Can melasma be prevented?
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Triluma Menu

  • About Tri-Luma® Cream
  • How to Use Tri-Luma® Cream
  • Safety & Side Effects
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  • What is melasma?
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About Melasma
What is melasma?
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Can melasma be prevented?

About Tri-Luma® Cream
About Tri-Luma® Cream
How to apply Tri-Luma® Cream
Who should not use Tri-Luma® Cream
What to expect from treatment with Tri-Luma® Cream
What to avoid while using Tri-Luma® Cream
Possible side effects of Tri-Luma® Cream
Stopping treatment with Tri-Luma® Cream
Where can I get Tri-Luma® Cream?
When does Tri-Luma® Cream begin working?
How long do the results last?

Learn more about Tri-Luma® Cream

IMPORTANT SAFETY INFORMATION
Indication: TRI‐LUMA® (fluocinolone acetonide 0.01%, hydroquinone 4%, tretinoin 0.05%) Cream is indicated for the short‐term (up to 8 weeks) treatment of moderate to severe melasma of the face in the presence of measures for sun avoidance, including the use of sunscreens. Adverse Events: In the controlled clinical trials, the most frequently reported events were redness, peeling, burning, dryness, and itching at the site of application. Warnings/Precautions: TRI‐LUMA® Cream contains sulfites which may cause severe, life‐threatening allergic reactions in people allergic to sulfites. TRI‐LUMA® Cream contains hydroquinone, which may cause a gradual blue‐black darkening of the skin. If you are pregnant, nursing or trying to become pregnant you should not use TRI‐LUMA® Cream. Safety and efficacy have not been established in individuals with darker skin. Reversible HPA axis (adrenal function) suppression may result from exposure to the topical corticosteroid, fluocinolone acetonide, so discontinue use if signs and symptoms of this condition occur. Avoid products that may dry or irritate the skin, such as abrasive cleansers, scrubs, or skin‐peeling agents. Exposure to sunlight, sunlamps, or UV light and extreme heat, wind, or cold should be avoided. If exposure cannot be avoided, sunscreen products [SPF 30 or more] and protective apparel should be used.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch, or call 1-800-FDA-1088.

*The Galderma® CAREConnectTM Program (“Program”) is brought to you by Galderma Laboratories, L.P. (“Galderma”). The Program is only available for commercially unrestricted or commercially restricted/cash paying patients at participating pharmacies. Patients who are enrolled in state or federally government-run or government-sponsored healthcare plan with a pharmacy benefit are not eligible to use the Galderma CAREConnect Patient Savings Card (“Card”). Any claim under the Program must be submitted by participating pharmacies to one of the Administrators of the Program.

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