LUCIDA PIGMENT CREAM PLUS

LUCIDA PIGMENT CREAM PLUS

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Description

Advanced Multi-Targeted Depigmenting Formula
Hydroquinone-based. Designed for melasma, PIH, and uneven pigmentation


Product Overview

Lucida Pigment Cream Plus is a physician-formulated cream designed to treat melasma, post-inflammatory hyperpigmentation (PIH), and UV-induced dark spots by targeting multiple biological pathways of melanogenesis. The formulation combines Hydroquinone, a gold-standard tyrosinase inhibitor, with Tranexamic Acid, Vitamin C, and Glycolic Acid to suppress pigment formation, exfoliate dyschromic cells, and reduce inflammatory triggers of melanocyte activation.

This multi-functional approach makes Lucida an ideal choice for short-term intensive protocols or as part of staged treatment plans for persistent pigmentary disorders.


Core Mechanisms of Action

  • Hydroquinone (HQ):
    Inhibits tyrosinase, the rate-limiting enzyme in melanin production. HQ is most effective in treating epidermal pigmentation and has rapid onset of action in reducing hyperchromia.

  • Tranexamic Acid (TA):
    Reduces UV- and inflammation-induced pigmentation by interfering with the plasminogen activation system. TA downregulates prostaglandins and arachidonic acid pathways, indirectly reducing melanocyte overactivity.

  • Vitamin C (L-Ascorbic Acid or derivative):
    A potent antioxidant that scavenges reactive oxygen species (ROS), slows melanin synthesis, and improves collagen quality. It also enhances skin luminosity.

  • Glycolic Acid (AHA):
    Improves epidermal turnover, facilitates penetration of depigmenting agents, and accelerates the shedding of pigmented keratinocytes. Supports mild resurfacing and skin texture refinement.


Clinical Indications

  • Epidermal melasma (symmetric, light-to-moderate depth)

  • Post-inflammatory hyperpigmentation (acne, friction, burns, cosmetic irritation)

  • Sun-induced lentigines and photodamage

  • Adjuvant use in protocols including laser toning, microneedling, and chemical peels

  • Early-stage pigmentation in combination with oral TA (under specialist care)


Recommended Use in Clinical Settings

  • Application:
    Apply once daily at night on cleansed, dry skin. Spot-treat on pigmented areas or apply to the full face depending on the distribution of lesions.

  • Duration:
    Use for a maximum of 12–16 weeks as part of a pigment correction phase. Follow with a maintenance regimen using non-HQ brighteners (e.g., arbutin, niacinamide, kojic acid).

  • Sunscreen:
    A broad-spectrum SPF 50+ is mandatory in the morning and throughout the day to prevent rebound pigmentation and irritation.

  • Titration & Monitoring:
    Start every other night in sensitive patients (Fitzpatrick IV–VI), increase to nightly as tolerated. Assess response at 4, 8, and 12 weeks.


Clinical Tips for Optimal Use

  • Pair with barrier-strengthening moisturizers in patients with dry or reactive skin

  • Can be layered with in-office TA mesotherapy or combined with oral TA for faster results

  • Avoid concurrent use with strong retinoids or acids unless on a staggered schedule

  • Consider stopping HQ temporarily before chemical peels or laser treatments to reduce irritation risk


Contraindications

  • Pregnancy and breastfeeding

  • History of exogenous ochronosis or HQ allergy

  • Active eczema, barrier impairment, or open wounds in treatment area

  • Recent chemical exfoliation or resurfacing procedures (wait 7–14 days minimum)


Expected Skin Reactions

  • Mild peeling, tingling, dryness, or redness during the first 1–3 weeks

  • Temporary worsening of pigmentation may occur before improvement

  • In rare cases: irritation-induced rebound PIH or contact dermatitis
    → If observed, reduce frequency or pause until barrier stabilizes


Key Ingredients

Actives:

  • Hydroquinone (2% or 4%, depending on local regulations)

  • Tranexamic Acid

  • Vitamin C (stabilized form)

  • Glycolic Acid

Vehicle base includes:

  • Emollients, pH regulators, absorption enhancers, non-sensitizing preservatives.

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