SunBurnt PLUS Pain Relief
SunBurnt PLUS Pain Relief is an FDA drug label for the active ingredient LIDOCAINE HYDROCHLORIDE manufactured by Welmedix LLC dba Welmedix Consumer Healthcare 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 20180313.
- Generic name
- LIDOCAINE HYDROCHLORIDE
- Manufacturer
- Welmedix LLC dba Welmedix Consumer Healthcare
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 24330-240
- Application
- part348
- Label effective
- 20180313
About this product
SunBurnt PLUS Pain Relief is an FDA-registered drug product whose active ingredient is LIDOCAINE HYDROCHLORIDE. It is labelled by Welmedix LLC dba Welmedix Consumer Healthcare taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 24330-240, application part348, label effective 20180313. It is one of 110 FDA drug label records sharing the active ingredient LIDOCAINE HYDROCHLORIDE. 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 LIDOCAINE HYDROCHLORIDE are most often described in connection with: temporarily relieves, itching due, sunburn minor, burns insect, skin irritations, cuts scrapes. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Temporarily relieves pain and itching due to: sunburn minor burns insect bites minor skin irritations minor cuts scrapes
Dosage & Administration
Directions clean skin and apply to affected area adults and children 2 years of age and older: apply to affected area not more than 3-4 times daily children under 2 years of age: ask a doctor
Warnings
Warnings For external use only Do not use in large quantities, particularly over raw surfaces or blistered areas if you have an allergy or hypersensitivity to any ingredients Ask a doctor before use if you have severe sunburn you have a rash or broken or compromised skin When using this product avoid contact with eyes Stop use and ask a doctor if condition worsens symptoms last more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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View labelHow products containing LIDOCAINE HYDROCHLORIDE compare
FDA lists 110 drug label records with LIDOCAINE HYDROCHLORIDE 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 Purchasing Solutions, LLC | 18 |
| — | — | Asclemed USA, Inc. | 6 |
| — | — | Water-Jel Technologies | 6 |
| — | — | SKINS SEXUAL HEALTH LIMITED | 5 |
| — | — | Nantong Health & Beyond Hygienic Products Inc. | 4 |
Frequently asked questions
What is SunBurnt PLUS Pain Relief used for?
Uses Temporarily relieves pain and itching due to: sunburn minor burns insect bites minor skin irritations minor cuts scrapes
Who makes SunBurnt PLUS Pain Relief?
Welmedix LLC dba Welmedix Consumer Healthcare is the labeler of record for SunBurnt PLUS Pain Relief. 110 FDA label records share the active ingredient LIDOCAINE HYDROCHLORIDE, 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 SunBurnt PLUS Pain Relief 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 SunBurnt PLUS Pain Relief 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 LIDOCAINE HYDROCHLORIDE?
Yes. 110 FDA drug label records list LIDOCAINE HYDROCHLORIDE 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 SunBurnt PLUS Pain Relief 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.