Raylieve™ Pain Stick · 65 g
Menthol sticks haven't changed SINCE THE WALKMAN.
We changed them.

The first far-infrared emissive pain stick — pharmaceutical-grade menthol, methyl salicylate, arnica, ginger, and rosemary for the next ninety seconds, and a TiO₂ + silica FIR mineral matrix that keeps working on your tissue for the next several hours. Twist. Apply. Celebrate.

The Problem
Forty years. No progress.

Cooling is not healing.

Every menthol stick on the shelf runs the same play: activate TRPM8 cold receptors, create a distraction sensation, hope you forget the underlying problem for fifteen minutes. The pain isn't being treated. It's being out-shouted.

The cooling fades. Then what?

Within fifteen minutes the menthol has volatilized. The cold is gone. The joint stiffness, the muscle spasm, the inflammatory swelling, the restricted blood flow — all still there. Conventional sticks end the moment they were supposed to start working.

And your skin pays for it.

Petroleum bases. Alcohol-heavy carriers. Harsh chemical actives that dry, crack, and irritate the skin you keep applying them to. The product you trust with your pain is quietly degrading the tissue it touches.

"The opportunity was never a stronger menthol stick. It was a stick that gives you the next ninety seconds AND the next several hours — in one application."
The Dual Timeline
Two products. One application.

Raylieve™ Pain Stick delivers two distinct timelines simultaneously. The cooling you reach for in the moment. The FIR engine that keeps working long after.

Dual-timeline cooling and FIR handoff Menthol cooling peaks within 5 minutes and fades by 20 minutes. The FIR mineral matrix continues emitting for hours. Apply 5 min 20 min 1 hour Hours later COOLING PEAK FIR SUSTAINED Menthol + terpenes FIR mineral matrix
Layer 1 · 0–20 minutes

The Cooling You Reach For

Pharmaceutical-grade menthol activates TRPM8 cold receptors within seconds. Layered with methyl salicylate from wintergreen oil for deeper salicylate analgesia, arnica's sesquiterpene lactones for direct anti-inflammatory action, ginger's gingerols for a warming counterpoint, and rosemary's penetration-enhancing terpenes to drive everything deeper.

Layer 2 · Several hours

The Engine That Stays

After the menthol and salicylate volatilize, the FIR mineral matrix — titanium dioxide and silica — remains deposited on the skin. It absorbs your body's 37°C thermal radiation and re-emits it as far-infrared photons peaked near 9.4 µm — tuned to the vibrational absorption modes of liquid water. Powered entirely by you.

The Breakthrough
A wax-based carrier engineered to hold FIR minerals against your skin for hours.

The Raylieve™ mineral matrix — titanium dioxide and silica — is suspended in a lipid carrier of caprylic/capric triglyceride, beeswax, and sunflower seed oil that does three jobs at once. It deposits the minerals against the skin in a sustained-release film, it extends the cooling phase by slowing volatile evaporation, and it carries the active botanicals — arnica, wintergreen, ginger, rosemary — deep into the dermal layers where they need to go.

Because human tissue is roughly 70% water by mass, the deposited mineral matrix creates a direct resonant energy transfer from skin surface into interstitial fluid, connective tissue, and the microvascular bed — for hours after application. No battery. No charging. No session.

Critical distinction

This is NOT photobiomodulation. Red and NIR light therapies operate at 600–900nm and target cytochrome c oxidase in mitochondria. Raylieve™ operates at 3–14 microns through resonant water absorption — a fundamentally different mechanism, a different part of the spectrum, and a different biological pathway entirely.

5
Concurrent biological pathways
9.4µm
Peak FIR — O-H resonance
65g
Twist-up. Pocket. Glove box.
0
Petroleum · parabens · fragrance
How It Works
Five pathways. One stick.

No single-mechanism product — menthol-only, lidocaine, NSAID gel, capsaicin — can match this breadth of action in a portable format. Tap to expand each pathway.

01
Menthol — Immediate TRPM8 Activation
The cooling that signals relief in seconds
Sensory
Pharmaceutical-grade menthol binds TRPM8 cold-sensing receptors in cutaneous nerve endings within seconds. Produces the recognizable cooling sensation and engages descending inhibitory pain pathways in the spinal cord — the gate control mechanism. Mild local vasodilation through TRPM8-mediated nitric oxide release begins the circulation cascade the other pathways will amplify. Calibrated for therapeutic effect without skin irritation, suitable for repeated daily use.
02
Methyl Salicylate — Topical Salicylate Analgesia
From wintergreen oil. COX inhibition at the application site.
Analgesic
Wintergreen oil (Gaultheria procumbens) is approximately 85–98% methyl salicylate — a topical salicylate that hydrolyzes in the skin to salicylic acid, inhibiting cyclooxygenase (COX-1 and COX-2) and reducing local prostaglandin synthesis. This is mechanistically distinct from menthol's nerve-level distraction: methyl salicylate acts on the inflammatory pathway itself, attenuating the chemical signaling that generates pain. The salicylate also produces a deeper, warming counter-irritant sensation that complements menthol's surface cooling — the same combination found in classical topical analgesics, but here without the petroleum or alcohol carrier.
03
Arnica + Ginger — Botanical Anti-Inflammatory
Helenalin, sesquiterpene lactones, gingerols, zingiberene
Inflammatory
Arnica montana contributes helenalin and related sesquiterpene lactones, documented inhibitors of NF-κB transcription — the master switch for inflammatory gene expression. Arnica's traditional and clinical use for bruising, soft-tissue trauma, and muscle soreness rests on this mechanism. Ginger root oil (Zingiber officinale) layers on gingerols, zingiberene, and β-sesquiphellandrene, which inhibit COX and LOX enzymes through pathways independent of methyl salicylate's, providing convergent anti-inflammatory action plus a mild thermogenic effect that supports circulation. Two independent anti-inflammatory inputs hitting the same biology from different molecular angles.
04
FIR Emission — The Sustained Engine
TiO₂ + silica matrix. Body heat → 3–14 µm far-infrared, for hours.
Physics
After the volatile actives evaporate, the mineral matrix — titanium dioxide and silica — remains, continually absorbing body heat and re-emitting it as far-infrared photons across the 3–14 micron biological window. The TiO₂ and silica pair was chosen for their broadband emissivity in this range; silica's Si-O bond resonances and TiO₂'s phonon modes together cover the wavelengths where liquid water absorbs most strongly. The emission drives molecular reorganization of interfacial water, promotes expansion of Pollack-type exclusion zone (EZ) water at biological surfaces, and stimulates endothelial nitric oxide synthase (eNOS). Blood vessels relax. Microcirculation increases. For hours, not minutes.
05
Rosemary + Carrier — Aromatic Synergy and Sustained Release
1,8-cineole, camphor, α-pinene + caprylic/capric, beeswax, sunflower
Synergy
Rosemary oil contributes 1,8-cineole (eucalyptol), camphor, and α-pinene — terpenes with documented anti-inflammatory activity and, critically, penetration-enhancing effects that improve transdermal delivery of every other active in the stick. The carrier matrix — caprylic/capric triglyceride (medium-chain fatty acids that absorb rapidly), beeswax (creates the occlusive film that holds the FIR minerals against the skin), and sunflower seed oil (linoleic-acid-rich, supports the skin barrier) — is engineered to absorb cleanly without greasy residue while keeping the active complex in contact with the tissue for the full duration of the FIR phase. No petroleum. No synthetic fragrance. No parabens.
The Human Story

Forty minutes into a long drive, your lower back tightens up. You know what's coming.

The dull ache that will be a sharp ache by the time you reach the hotel. The sleepless night by the time you try to lie down. You shift in the seat. You arch your spine. It doesn't help.

You reach into the center console for the stick you've started keeping there. You twist it up. You pull your shirt aside at the next stoplight and run it across the worst of it — the spot at the base of your spine that always gives out first. It absorbs in seconds. No greasy residue on your hand. No medicinal smell filling the car. Just a clean, building coolness on the skin and a sense that something has actually been done.

And then — for the first time — the cooling fades into something else.

Ten minutes later, when a conventional menthol stick would already be fading, you notice the cooling is softening but the ache underneath is also softening. By the time you pull into the hotel, the menthol is gone and the cooling is gone — but the spot where you applied it is warmer than the surrounding skin, in a way you can feel without touching. That's the minerals working. That's the FIR pulling heat out of your own body and pushing it back into the tissue as infrared energy.

You walk to your room. You're not limping. You're not stiff. You don't reach for the stick again that night. In the morning, the spot that would normally be locked up feels closer to baseline than it has any right to be.

"Most pain sticks give you a sensation and call it a solution. Raylieve™ gives you physics, pharmacology, and skin science — in a stick."
Competitive Landscape
A category of one.

The Pain Stick does not have a direct competitor. It occupies space between five established categories — borrowing the best of each while carrying the limitations of none.

vs. Menthol SticksBiofreeze · Tiger Balm · Icy Hot · Salonpas

Chemical counter-irritation. Single mechanism. No sustained action after volatile actives evaporate. No skin benefit. Petroleum or alcohol-heavy bases. Raylieve delivers five concurrent biological pathways in the same portable format, with a skin-positive lipid carrier and hours of sustained FIR emission.

Same shelf. Different category.
vs. CBD + Cannabinoid TopicalsCBD roll-ons · cannabinoid balms

CBD topicals operate through CB2 receptor modulation and inherit a regulatory environment that limits claims by jurisdiction. Raylieve delivers a mechanistically broader, fully unrestricted alternative: methyl salicylate for direct COX inhibition, arnica's sesquiterpene lactones for NF-κB suppression, ginger's gingerols for independent COX/LOX inhibition, plus sustained FIR emission — four independent anti-inflammatory and analgesic pathways, no regulatory baggage.

Broader chemistry. No regulatory ceiling.
vs. Lidocaine Patches + Roll-OnsAspercreme Lidocaine · Salonpas Lidocaine

Lidocaine numbs cutaneous nerves but does nothing to the underlying tissue. No circulation effect. No inflammation reduction. No tissue repair. Raylieve produces immediate sensory relief through a non-anesthetic mechanism while simultaneously driving the deeper biological work lidocaine cannot touch.

Sensation plus substance. Not sensation alone.
vs. CELLIANT + FIR TextilesFIR sleeves · socks · bedding

Closest conceptual parallel — FIR-emitting minerals that absorb body heat. But CELLIANT is a textile technology. Sleeves, socks, bedding. No topical applications. No acute-relief format. CELLIANT built the FIR category. Raylieve™ is the portable, on-body, acute-use format the textile category cannot deliver.

They opened the door. We applied it directly to the skin.
vs. Powered DevicesTENS units · red light wraps · heating pads

Powered devices require electronics, batteries, charging, sessions, physical setup. Effective for some users — but unsuitable for the moment of acute pain in the field. At the trailhead. In the gym. Between meetings. In the car. Raylieve™ delivers sustained therapeutic energy with no device, no charging, no session.

Apply and go. Powered by your own thermal energy.

Ready to feel the handoff?

Free shipping · 30-day guarantee · One technology, two formats