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Meet Ultra Refining Lytic Serum: Redefining Radiance
Barrier Care Before It Was Cool: The Epionce Story
How to Layer Skincare for A Healthy Skin Barrier
The Missing Step in Your Skincare Routine

Meet Ultra Refining Lytic Serum: Barrier-Safe Botanical Exfoliant for Radiant, Refined Skin

September 22, 2026

supporting-skin

Supporting Skin

How to Layer Skincare for A Healthy Skin Barrier

September 1, 2026

antiaging

Anti-Aging

The Missing Step in Your Skincare Routine

August 19, 2026

supporting-skin

Supporting Skin

Spoiler Alert: “Glass Skin” is Healthy, Hydrated Skin

July 30, 2026

epionce-skincare

Epionce Skin Care

Sports and Skincare: How to Support Your Skin Barrier When You’re Active

July 17, 2026

supporting-skin

Supporting Skin

Why Your Skin Barrier and Microbiome Matter for Healthy Aging

July 1, 2026

skin-barrier

skin barrier

The Truth About Ceramides: Your Skin Barrier Needs More Than That

June 17, 2026

dry-skin

dry skin

Skincare Is NOT One Size Fits All

June 2, 2026

supporting-skin

Supporting Skin

Razor Bumps, Ingrown Hairs, or Razor Burn? Here’s How to Tell the Difference

May 21, 2026

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beard care

Are LED Face Masks Overhyped? Here’s the Truth

April 27, 2026

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clinically proven

Spring Skin Reset: Why Seasonal Changes Call for Head-to-Toe Hydration

April 8, 2026

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Supporting Skin

Biomimetic Skin Care: Supporting Your Skin Barrier Without Irritation

March 17, 2026

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skin barrier

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The U.S. Food and Drug Administration (FDA) defines cosmetics as "articles...applied to the human body...for cleansing, beautifying, promoting attractiveness, or altering the appearance." The majority of Epionce® products described on this website are intended to meet this definition. These Epionce® products and their associated statements have not been approved or evaluated by the FDA and are not intended to be drug products that diagnose, treat, cure, or prevent any disease or condition.

Epionce Daily Shield Tinted SPF 50 is considered an over-the-counter drug product. It is formulated and marketed pursuant to the FDA’s governing regulations set forth at 21 C.F.R. Part 352.

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