Peptide Therapy · SELANK· Serving South Metro Denver

No. Selank is not FDA-approved to treat anxiety or any other psychiatric condition in the United States. Although it has been researched for anxiety-related effects, it should not replace prescribed mental-health treatment.

Selank is generally researched for calming effects without traditional sedation. Individual responses can vary, however, and its safety and effects have not been established through large U.S. clinical trials.

There is no established timeline for response. Individual experiences may vary depending on the formulation, protocol, baseline health, and treatment goals.

Potential medication interactions should be reviewed by a qualified provider before use. Clients should disclose antidepressants, anti-anxiety medications, stimulants, sleep medications, and other medications or supplements during their medical evaluation.

We kindly ask for at least 24 hours’ notice to cancel or reschedule your appointment. Cancellations within 24 hours will incur a 50% fee. If we arrive and are unable to reach you or access the appointment location after a brief grace period, the visit will be considered a no-show and may be charged up to the full service amount. Same-day bookings require a minimum of 4 hours’ notice for any changes. As each appointment is reserved exclusively for you — including provider time and travel — we appreciate your understanding.

Pregnancy or breastfeeding, certain medical or psychiatric conditions, medication interactions, allergies, or other individual risk factors may affect candidacy. A medical evaluation should be completed before treatment.

No. Selank is not FDA-approved in the United States for anxiety, cognitive enhancement, stress management, or other therapeutic uses.

There is no established treatment timeline, and individual response can vary based on baseline skin tone, genetics, dose, and other factors. Changes in pigmentation may develop gradually rather than immediately.

Yes. Increased pigmentation does not eliminate the risk of UV-related skin damage or skin cancer. Broad-spectrum sunscreen and appropriate sun-protective measures remain important.

Melanotan II can increase pigmentation, but intentional UV exposure carries established risks and should not be considered “safe” because Melanotan II is being used. We would avoid positioning tanning beds or additional UV exposure as part of the treatment protocol.

It can increase pigmentation of existing freckles, moles, and other pigmented areas. Any new, rapidly changing, irregular, bleeding, itching, or otherwise concerning lesion should be evaluated by a qualified dermatology provider.

We kindly ask for at least 24 hours’ notice to cancel or reschedule your appointment. Cancellations within 24 hours will incur a 50% fee. If we arrive and are unable to reach you or access the appointment location after a brief grace period, the visit will be considered a no-show and may be charged up to the full service amount. Same-day bookings require a minimum of 4 hours’ notice for any changes. As each appointment is reserved exclusively for you — including provider time and travel — we appreciate your understanding.

Candidacy requires individualized medical evaluation. A history of melanoma or other skin cancers, atypical/dysplastic nevi, concerning pigmented lesions, pregnancy or breastfeeding, or certain medical conditions may make treatment inappropriate or warrant additional evaluation.

Reported effects can include nausea, flushing, decreased appetite, headache, fatigue, increased pigmentation of freckles or moles, and changes in libido or spontaneous erections. Because Melanotan II is investigational, its complete long-term safety profile has not been established.