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SYS · ONLINEPASS · 63.0%
Open Assay
Independent Testing / Est. 2026
BATCH04·26·B
PASS63.0%
N27
PeptidesCosmeticAcetyl Tetrapeptide-5

Acetyl Tetrapeptide-5

/ Synthetic acetylated tetrapeptide; INCI 'Acetyl Tetrapeptide-5'; periorbital edema / under-eye cosmetic peptide
SPECULATIVEN = 0 · TESTING PENDING

ALIAS · Eyeseryl (trade — Lipotec) · Acetyl Tetrapeptide-5 (INCI)

Pass rate
0
Samples
0
Suppliers
Research use onlyAny dose figures below describe what specific cited studies used, reported factually. Nothing on this page is guidance for human use.READ FIRST →

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§ A · Identity
Primary sequence— sequence not captured —
MW · CLASS · Synthetic acetylated tetrapeptide; INCI 'Acetyl Tetrapeptide-5'; periorbital edema / under-eye cosmetic peptideCATEGORY · Cosmetic

Tier 4 cosmeceutical. INCI catalog peptide marketed under the Eyeseryl trade name (Lipotec / Lubrizol) for periorbital edema and under-eye puffiness. Supplier-published topical clinical material exists; independent Western placebo-controlled replication is limited.

§ B · Mechanism of action

The supplier-stated mechanism is inhibition of angiotensin-converting enzyme (ACE) activity in periorbital microvasculature, with downstream effects on vascular permeability and local fluid retention that are positioned as drivers of under-eye puffiness and dark-circle appearance. Topical penetration of a four-residue peptide to capillary-bed depth is the central uncertainty — formulation (liposomes, gels) is the principal variable in any reported effect.

§ C · Human clinical evidence

Tier 4. Supplier-published topical studies (Lipotec / Lubrizol) report reductions in periorbital edema and under-eye dark-circle scoring versus vehicle in subject panels of modest size. PubMed-indexed independent replication is sparse.

§ F · Safety signal

Topical application in cosmetic formulations is reported as well tolerated. No systemic exposure has been characterised; ophthalmic safety has not been formally assessed as it would be for a drug product, given the close-to-eye application area.

§ H · Regulatory status

Regulatory status

FDA status:
Not FDA-approved
§ I · Notable gaps and controversies

Industry-authored efficacy framing dominates the published record. The ACE-inhibition mechanism is plausible at the molecular level but is not directly demonstrated in human periorbital tissue post-topical-application. Cosmeceutical positioning is not subject to the FDA drug-efficacy review that would test such mechanism claims.