Numbing Pain Relief
Numbing Pain Relief is an FDA drug label for the active ingredient LIDOCAINE 4% manufactured by Walgreen Company 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 20260722.
- Generic name
- LIDOCAINE 4%
- Manufacturer
- Walgreen Company
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 0363-6261
- Application
- M017
- Label effective
- 20260722
About this product
Numbing Pain Relief is an FDA-registered drug product whose active ingredient is LIDOCAINE 4%. It is labelled by Walgreen Company taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 0363-6261, application M017, label effective 20260722. It is one of 31 FDA drug label records sharing the active ingredient LIDOCAINE 4%. 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 4% are most often described in connection with: temporarily relieves, itching associated, minor burns, cuts scrapes, insect bites, skin irritations. 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 associated with minor burns, sunburn, minor cuts, scrapes, insect bites, or minor skin irritations
Dosage & Administration
Directions Adults and children 2 years of age and older Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age do not use, consult a doctor
Warnings
For external use only In large quantities, particularly over raw surfaces or blistered areas Do not allow contact with the eyes condition worsens symptoms last more than 7 days or clear up and occur again within a few days If pregnant or breast feeding, ask a health professional before use. 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 4% compare
FDA lists 31 drug label records with LIDOCAINE 4% 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 |
|---|---|---|---|
| — | — | Jiangxi Yudexi Pharmaceutical Co., LTD | 10 |
| — | — | Walgreens | 3 |
| — | — | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 3 |
| — | — | Guangxi Keyun E-commerce Co., Ltd. | 2 |
| — | — | Asclemed USA, Inc. | 1 |
Frequently asked questions
What is Numbing Pain Relief used for?
Uses Temporarily relieves pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, or minor skin irritations
Who makes Numbing Pain Relief?
Walgreen Company is the labeler of record for Numbing Pain Relief. 31 FDA label records share the active ingredient LIDOCAINE 4%, 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 Numbing 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 Numbing 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 4%?
Yes. 31 FDA drug label records list LIDOCAINE 4% 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 Numbing 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.