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For Plastic Surgeons & Aesthetic Providers

A Post-Procedure Skincare Protocol
Your Patients Will Actually Use

CODE3 delivers Tranexamic Acid, Bakuchiol, and Quercetin in a single, fragrance-free formula — refined over 12 years and 2,500+ patients by a board-certified plastic surgeon who needed it in his own practice.

Formulated by a board-certified plastic surgeon
Refined over 12 years, across 2,500+ patients
Patent Pending
Formulated By

Dr. Daniel Jacobs, MD — Plastic Surgeon & Founder, Alón Labs

Dr. Jacobs developed CODE3 over 12 years of clinical use across more than 2,500 patients, refining the formula specifically for the post-procedure window when standard actives are contraindicated — with particular attention to higher-Fitzpatrick patients at elevated PIH risk and to the day 1–14 healing-skin constraint.

The Clinical Rationale for Each Active

Post-procedure skin faces one primary threat: melanocyte overactivation via the plasmin pathway, driving post-inflammatory hyperpigmentation (PIH). CODE3 addresses this with three synergistic actives — each with independent peer-reviewed support — in concentrations proven effective on healing skin.

Active 01
Tranexamic Acid
Pigment-correction concentration

Inhibits plasmin upstream of melanogenesis, blocking the plasminogen–keratinocyte interaction that drives melanocyte activation after trauma. Controlled trials report efficacy comparable to hydroquinone for melasma and PIH — without the bleaching mechanism, irritation profile, or prescription requirement (PMID 38918942; PMID 39045920). Well-tolerated on re-epithelializing skin from day 5 post-procedure.

Active 02
Bakuchiol
Clinically active concentration

Produces retinoid-functional effects on collagen synthesis and epidermal remodeling without photosensitization. A 2018 double-blind BJD trial (Dhaliwal et al., PMID 29947134) compared bakuchiol 0.5% twice daily with retinol 0.5% once daily over 12 weeks; both groups showed comparable improvement in photoaging and fine lines, and bakuchiol users reported less facial scaling and stinging. A well-tolerated option when retinol is contraindicated post-procedure (PMID 33346506).

Active 03
Quercetin
Synergistic antioxidant

Addresses the third pathway in the platform: oxidative stress. Neutralizes the post-procedure free-radical burst and downregulates NF-κB inflammatory signaling — closing the loop on the inflammation that would otherwise amplify melanocyte activation and undercut TXA's effect. No irritation or sensitization risk on compromised skin.

How CODE3 Compares

CODE3 is formulated for the specific window when standard actives are contraindicated — and for patients who cannot tolerate or do not want prescription options.

Property Hydroquinone 4% Retinol 0.5% CODE3 (TXA + Bakuchiol + Quercetin)
Prescription required Yes (US, >2%) No No
Safe post-procedure No — avoid on healing skin No — photosensitization risk Yes — from day 5 post-procedure
PIH prevention mechanism Bleaching (melanin inhibition) Indirect (cell turnover) Plasmin reduction (upstream of melanogenesis)
Collagen stimulation No Yes Yes (via Bakuchiol)
Fitzpatrick III–VI tolerability Variable — rebound risk Poor — irritation at darker tones Well-tolerated across all skin types
Fragrance-free Varies by formulation Varies Yes

When to Recommend CODE3

Procedure Start TXA + Bakuchiol Continue Through
Fractional LaserDay 5–7Week 8
Ablative Laser (CO₂ / Er:YAG)Day 10–14Week 10–12
Medium Chemical Peel (TCA)Day 7–10Week 8
Superficial Peel (Glycolic / Mandelic)Day 3–5Week 6
Microneedling (0.5–1.5 mm)Day 3–4Week 6
IPL PhotofacialDay 3–5Week 6
Rhinoplasty / Facelift (skin prep)4 weeks pre-opWeek 8 post-op

What to Tell Your Patients

Scripted language your team can use at discharge or during post-op calls.

Patient Talking Points

On why they need a specific skincare product now:

"Your procedure activated the cells that produce pigment. If we don't interrupt that signal right away, you can develop dark spots that are harder to treat than what we addressed today. This formula does that without irritating your healing skin."

On why not to use their existing retinol or hydroquinone:

"Retinol increases cell turnover and causes photosensitivity — both problems while your skin is healing. Hydroquinone isn't formulated for healing skin. CODE3 achieves the same clinical goal through a different mechanism that's safe to use now."

On when to start:

"Once the surface of your skin is intact — no raw areas — you can start. For most patients after [procedure], that's around day [X]. Apply morning and evening as directed."

Stock CODE3 in Your Practice

Available for wholesale. Request samples, pricing information, and patient handout materials.

Frequently Asked Questions

Yes. The formula is fragrance-free and non-comedogenic, formulated without common sensitizers. The Tranexamic Acid mechanism is particularly relevant for Fitzpatrick III–VI patients who carry the highest PIH risk post-procedure.
Yes. CODE3 is designed to layer cleanly under mineral SPF. Apply morning and evening after cleansing, before sunscreen in the morning routine. No compatibility concerns with standard post-procedure cleansers or physical sunscreens.
Contact skin-science@alonlabs.com for wholesale pricing and minimum order information. Sample kits are available for evaluation prior to purchase.
No prescription is required. CODE3 is a cosmetic product formulated for topical use.
CODE3 is a three-active combination — Tranexamic Acid, Bakuchiol, and Quercetin — calibrated for the post-procedure window. The TXA concentration is at the upper end of the range used in topical clinical trials for melasma and PIH; many OTC serums use 2–3%.
Yes. A 2018 double-blind RCT in the British Journal of Dermatology (Dhaliwal et al., PMID 29947134) compared bakuchiol 0.5% twice daily with retinol 0.5% once daily over 12 weeks. Both groups showed comparable improvement in photoaging and fine lines, and bakuchiol users reported less facial scaling and stinging.

This page is intended for licensed healthcare professionals. CODE3 is a cosmetic product, not a drug. Clinical references are provided for informational purposes. Individual patient results will vary. These statements have not been evaluated by the FDA. Consult current clinical literature for patient care decisions.