Product identity

What was that, exactly?

Type the name as it was said to you or printed on the box — or a number from it: an NDC, a device identifier or full UDI, a 510(k), PMA or application number. A name is matched against this site’s registry; a number can be looked up in FDA’s own records, with any recall filed under it. A match says a record exists. It never says the vial or device in front of you is that product.

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Registry match

Restylane Eyelight

Galderma Laboratories, L.P. · Hyaluronic acid fillers

FDA-approved medical device (PMA)P040024/S135

What it’s authorized for

Improvement of hollow areas under the eyes (infraorbital hollowing), in people 21 and older

Checking it’s the real thing

FDA advises not buying dermal fillers online (they could be counterfeit or not approved for U.S. use) and urges providers to inspect filler packages for authenticity. Page content current as of 2023-07-06.
FDA: Dermal Fillers (Soft Tissue Fillers) (opens in a new tab)
FDA consumer update: the provider should use properly labeled, sealed vials or pre-filled syringes of FDA-approved filler; do not buy fillers sold directly to the public or use needle-free injection pens. Content current as of 2023-07-07.
fda.gov/consumers/consumer-updates/dermal-filler-dos-and-donts-wrinkles-lips-and-more (opens in a new tab)

Checked Sep 14, 2026

Full page: label warnings, how it’s sold, sources

Official records

This looks like a PMA number.

Look it up in FDA and National Library of Medicine databases: the record it belongs to, who holds it, and any recall or enforcement report filed under it.

Sends only “P040024/S135” to this site, which asks FDA and the National Library of Medicine. Nothing else on this page or in your Booking File is sent, and nothing is stored.

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