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Start here · EDITORIAL DRAFT

Cosmetic, prescription or experimental?

Understand the differences before comparing two peptide products.

Sources checked October 20, 2026 · US context · Human editorial and scientific review pending

The short answer

A peptide name alone does not tell you whether a product is a cosmetic, an authorized medicine or an experimental preparation. Intended use and the specific product matter.[1]

Cosmetics: read the formula

Cosmetics concern cleansing or appearance. Treatment claims can change a product’s legal classification; a cosmetic ingredient is not automatically a medicine.[1]

Medicines: check the exact authorization

Do not transfer an authorized medicine’s status to a compounded version or an online vial. FDA says compounded GLP-1 preparations do not undergo the same approval review.[2]

Experimental: distinguish a trial from an offer

A study is not a retail product approval. For example, FDA says retatrutide is not a component of an approved drug. A seller’s research-only label does not verify quality.[2]

Compare products within their actual use and evidence context. Peptivelo’s commercial comparator currently covers cosmetic serums.

References and access limitsStudy design, commercial context and what was inspected
  1. Regulatory guidanceIs It a Cosmetic, a Drug, or Both?

    US FDA · Reference checked

    Evidence and limitations for reference 1
    What this supports here
    The US regulator’s stated distinction or risk communication at the inspection date.
    What it cannot establish
    Not a new clinical trial or a complete literature review. Regulatory statements have a jurisdiction, date and specific scope; absence of established safety is not proof of a particular injury.
    Commercial context and disclosures
    US government regulator; not a retailer.
    What we inspected
    Public source text inspected; underlying clinical dossiers not independently reanalysed.
  2. Regulatory guidanceFDA’s Concerns with Unapproved GLP-1 Drugs Used for Weight Loss

    US FDA · Reference checked

    Evidence and limitations for reference 2
    What this supports here
    The US regulator’s stated distinction or risk communication at the inspection date.
    What it cannot establish
    Not a new clinical trial or a complete literature review. Regulatory statements have a jurisdiction, date and specific scope; absence of established safety is not proof of a particular injury.
    Commercial context and disclosures
    US government regulator; not a retailer.
    What we inspected
    Public source text inspected; underlying clinical dossiers not independently reanalysed.
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