Oopsie 3 Hydrogen Peroxide
Oopsie 3 Hydrogen Peroxide is an FDA drug label for the active ingredient HYDROGEN PEROXIDE manufactured by 4 Visions LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260430.
- Generic name
- HYDROGEN PEROXIDE
- Manufacturer
- 4 Visions LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87251-006
- Application
- M003
- Label effective
- 20260430
About this product
Oopsie 3 Hydrogen Peroxide is an FDA-registered drug product whose active ingredient is HYDROGEN PEROXIDE. It is labelled by 4 Visions LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87251-006, application M003, label effective 20260430. It is one of 28 FDA drug label records sharing the active ingredient HYDROGEN PEROXIDE. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing HYDROGEN PEROXIDE are most often described in connection with: first aid, help prevent, risk infection, minor cuts. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses First aid to help prevent the risk of infection in minor cuts, scrapes and burns
Dosage & Administration
Directions clean the affected area spray a small amount of product on the affected area 1 to 3 times a day may be covered with a sterile bandage if bandaged, let dry first
Warnings
Warnings For external use only Do not use in the eyes or apply over large areas of the body longer than 1 week. Ask a doctor before use if you have deep or puncture wounds, animals bites or serious burns Stop use and ask a doctor if the condition persists or gets worse irritation, pain, or redness persists or worsens swelling, rash, or fever develops Keep out of reach of children. Is swallowed, get medical help or contact a Poison Control Center right away
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View labelHow products containing HYDROGEN PEROXIDE compare
FDA lists 28 drug label records with HYDROGEN PEROXIDE as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Medical Chemical Corporation | 2 |
| — | — | P & L Development, LLC | 2 |
| — | — | Strategic Sourcing Services LLC | 2 |
| — | — | 4 Visions LLC | 1 |
| — | — | Aero Healthcare US LLC | 1 |
Frequently asked questions
What is Oopsie 3 Hydrogen Peroxide used for?
Uses First aid to help prevent the risk of infection in minor cuts, scrapes and burns
Who makes Oopsie 3 Hydrogen Peroxide?
4 Visions LLC is the labeler of record for Oopsie 3 Hydrogen Peroxide. 28 FDA label records share the active ingredient HYDROGEN PEROXIDE, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.
What form does Oopsie 3 Hydrogen Peroxide come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Oopsie 3 Hydrogen Peroxide prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Are there other products containing HYDROGEN PEROXIDE?
Yes. 28 FDA drug label records list HYDROGEN PEROXIDE as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.
Has Oopsie 3 Hydrogen Peroxide been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.