
Extract the specific claim
Keep the exact product name, formulation if identified, publisher, date and a short statement of the claimed purpose. Distinguish appearance or cleansing claims from claims about treating disease or changing body structure or function. Do not assume every skin product has the same regulatory category, or that a herbal ingredient establishes safety and effectiveness for a particular person.
Read intended use in its jurisdiction
FDA explains that intended use helps determine whether a product is a cosmetic, a drug, both or another category under US rules. Keep that named context clear rather than presenting it as every country’s classification system. A retailer’s cosmetic heading does not by itself settle the status of a therapeutic claim. Ask the appropriate regulator or qualified professional about an unclear product.
Match evidence to the product and use
Keep a study about an ingredient separate from evidence about the exact marketed product and claimed use. Record the actual regulator record supplied, if any, and whether it matches. A scientific reference, customer testimonial or natural label is not a substitute for that match. Do not describe an unverified product as approved because a different formulation or ingredient appears elsewhere.
Take the personal question to a professional
For a treatment decision, symptoms, interactions or adverse effects, use an appropriate clinician or pharmacist rather than a marketing comparison. Retain the real label and relevant questions privately. This guide supplies no skin application schedule, medicinal dose, injection technique or procedure. If a claim cannot be traced, record evidence not located rather than turning uncertainty into a recommendation.
Read the drawing as text
A cosmetics heading, therapeutic claim and ingredient paper are different evidence. Match the exact product and use to the relevant regulatory record.
Work through an example
A fictional cream C is presented under a cosmetics heading but its advertisement claims to treat condition D. The reader records the therapeutic claim separately and asks for the exact applicable regulator record. A paper about ingredient I does not fill that missing link. No real product is classified, approved, rejected or recommended, and no treatment is demonstrated.
Illustrative example; figures, people and organisations in the worked record are fictional.
The example record
Product
- Evidence
- C / exact label requested
- Next question
- Which formulation?
Intended use
- Evidence
- Treatment of D claimed
- Next question
- Not just a shop category
Evidence
- Evidence
- Paper about ingredient I
- Next question
- Matches C and claimed use?
Regulator
- Evidence
- No matching record supplied
- Next question
- Status remains unverified
Download blank worksheet (.csv) ↗Download worked example (.csv) ↗
Keep your own record
Use the result within its scope
Use the actual regulator and qualified advice for the product and jurisdiction. This record clarifies a claim’s scope; it cannot determine clinical suitability or turn an ingredient citation into product approval.
Reference sources
Earlier articles on this subject
- Best Pain Relief Herbal Products With Multiple Benefits ↗ — 2022-07-26, Maria Baldwin.
- Important Information About Tattoos in San Jose ↗ — 2021-06-24, Maria Baldwin.
- Eyebrow Extensions Handle It Well To Enjoy The Advantages! ↗ — 2022-01-19, Maria Baldwin.