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Short answer: a liquid bandage is a sterile liquid that is spread over the top of a minor cut and left to dry, so that it covers the opening in the skin. MedlinePlus (NIH) describes it as a way to close a minor cut and help stop bleeding, with a waterproof seal that lasts about 5 to 10 days. This page explains what the product is under FDA rules, how it works, and how it differs from clinical tissue adhesives and sutures.
General product information only, not medical advice. Always follow the instructions on the product you are using.
What a liquid bandage is
The FDA defines a liquid bandage in 21 CFR 880.5090 (checked 2026-10-30) as “a sterile device that is a liquid, semiliquid, or powder and liquid combination used to cover an opening in the skin or as a dressing for burns,” and says it is also used as a topical skin protectant. It is a Class I device (general controls). When it is used only as a skin protectant, it is exempt from premarket notification (510(k)).
In FDA’s device database the category carries product code KMF, device name “Bandage, Liquid,” class 1, regulation number 880.5090 (openFDA classification record, checked 2026-10-30). As one example of a record in this category, openFDA lists a 510(k) for a BAND-AID Brand Liquid Bandage from Johnson & Johnson Consumer Companies, decided 2006-12-11 as substantially equivalent (K062602). That record shows the category exists; it says nothing about what is on sale today.
How does liquid bandage work?
A liquid bandage is spread as a liquid over the top of the skin along a minor cut. It then dries into a seal over the cut. MedlinePlus states that it goes on top of the skin, not inside the wound. Once dry it is waterproof, and the seal lasts about 5 to 10 days before it falls off by itself.
Products differ in their ingredients and in how they are labeled, so the label of the product you hold governs how it is used.
Does liquid bandage work?
For a minor cut, MedlinePlus says a liquid bandage can be used to close the wound and help stop bleeding, and that one application seals the cut. It also says that if the wound is thoroughly cleaned and rinsed first there is less chance of later infection because the wound is sealed shut, and that using these products may also reduce the size of scars.
The same source lists limits on the product itself: it is not meant for use around the eyes, in the ear or nose, or internally in the mouth, and it is described as a product for minor cuts rather than large ones. Consult the product label and a health care provider for questions about a particular wound.
Liquid bandage, tissue adhesive and sutures
People often use “skin glue” and “liquid bandage” for the same thing, but FDA’s regulation of a liquid bandage (Class I, a cover for an opening in the skin) is a separate matter from the clinical tissue adhesives and sutures used by professionals to close wounds. For those, see CASRAI’s guides to Dermabond and Prineo, Exofin and sutures. For the wider family of coverings, see what a bandage is and what a wound dressing is. Medical bandages are also listed in the bandages category at lac.us.
FAQ
How does liquid bandage work?
It is spread as a liquid over the top of a minor cut and dries into a waterproof seal that covers the opening in the skin.
Does liquid bandage work?
For minor cuts, MedlinePlus says it can close the cut and help stop bleeding. It is not meant for large cuts or for use near the eyes, ears, nose or inside the mouth.
How long does a liquid bandage last?
MedlinePlus says the seal lasts about 5 to 10 days and falls off naturally.
Is a liquid bandage waterproof?
Yes, once it has dried. MedlinePlus says these products are waterproof.
Is a liquid bandage regulated by FDA?
Yes. 21 CFR 880.5090 classifies it as a Class I device, with a premarket notification exemption when it is used only as a skin protectant.
Sources
- MedlinePlus (NIH, National Library of Medicine), “Skin glue / liquid bandage” patient instructions, https://medlineplus.gov/ency/patientinstructions/000497.htm, checked 2026-10-30.
- 21 CFR 880.5090, Liquid bandage, https://www.law.cornell.edu/cfr/text/21/880.5090, checked 2026-10-30.
- FDA openFDA device classification (product code KMF) and 510(k) record K062602, https://api.fda.gov/device/classification.json?search=product_code:KMF, checked 2026-10-30.








