~$2,900 per year
Product liability
- Introduced under AICIS registration, dermatologically tested
- Australian formulation, overseas manufacture
- All standard markets declined
- Placed to enable retail launch
Product classification and the claims made in advertising matter as much as the ingredient list. Appetite is selective, so the submission has to be precise.
Specialist
Market access
Hard-to-place
Our focus
Australia
National broking
Recognition
Peptide, cosmetic and skincare risks can be insurable, but appetite is selective and can change quickly. The submission needs the product and ingredient list, intended use, claims, regulatory pathway, quality evidence, suppliers, testing, labels, complaints and countries assembled before appetite is tested.
A product marketed as cosmetic can move toward therapeutic-goods territory when its intended use or advertising claims change. The business should distinguish its TGA, AICIS and other obligations product by product rather than relying on a broad category label.
The regulatory and underwriting classification of a skincare or peptide product follows its intended use and the claims made about it, not just the formulation. A moisturiser is a cosmetic; the same formulation marketed as treating a skin condition starts to look like a therapeutic good, with different obligations and a different insurance conversation.
Underwriters read labels, websites, social media and practitioner materials against the formal regulatory position. Inconsistency between them is one of the fastest ways to lose an otherwise placeable risk.
The product story has to stay consistent across formulation, label, website, customer pathway and regulatory position - and it has to stay consistent over time, because a claim made in one campaign can be quoted back at claim time.
Claims about treating, preventing or modifying health conditions can alter regulatory and underwriting classification. 'Cosmetic' is a claims discipline, not just a category.
Certificates of analysis, supplier quality and ingredient legality support the submission. For peptides specifically, underwriters commonly want product-by-product status, pathway and manufacturing controls rather than a category-level answer.
GMP evidence, batch release, stability data and temperature controls matter wherever product integrity can deteriorate between manufacture and customer.
Prescription, practitioner, wholesale and direct-to-consumer channels create different responsibilities and different severity. D2C sale of active products is priced accordingly.
Tell us what you advise on, build, test, supply or operate. We take the risk to insurers with genuine life sciences appetite and explain the terms before you decide.
Two anonymised consumer-product placements that show what specialist markets can do when the submission is complete.
~$2,900 per year
Product liability
~$1,200 per year
$20M public + products
Historical premiums from real Tank placements, rounded up and anonymised. They are evidence, not quotes - a different profile, or the same profile a year later, can price differently.
Every product, ingredient, concentration and intended use
The claims appearing on labels, websites, social media and practitioner material
The TGA, AICIS or other pathway applying to each product
Who manufactures, releases and tests each batch
Cold chain, complaints, adverse-event and recall controls
Supplier indemnities, insurance and rights of recourse
Peptide risks can face restricted appetite even with detailed controls. Early market testing beats late surprises.
Regulatory obligations sit outside your insurance policy. These official sources are the starting point.
External government and industry sources. Tank Insurance is not responsible for their content; confirm current requirements with the relevant body.
Potentially, but market appetite can be narrow and change quickly. Detailed product, regulatory, quality and supply-chain evidence is essential, and underwriters commonly assess product by product rather than by category.
No. Ingredients, intended use, claims, contamination potential, users, countries and manufacturing controls all matter. A cosmetic sold to infants can be priced above a simple therapeutic product.
Supplier or laboratory evidence about a material or batch. Underwriters use it alongside broader quality and testing controls to assess ingredient and manufacturing risk.
They show how customers are invited to use and rely on the product, and they can differ from the formal regulatory description. Underwriters and regulators both read them.
General information only. This page does not take account of your objectives, financial situation or needs and is not legal advice. Cover depends on the insurer, policy wording, limits, excesses, exclusions and information disclosed. Read the relevant policy documents and obtain professional advice before deciding.
Tell us what you research, build, test, supply or operate, plus any overseas exposure. We will explain the available terms and exclusions before you decide.
Last updated: 08/08/2026