Dr. Numb
Dr. Numb is an FDA drug label for the active ingredient LIDOCAINE manufactured by Shinpharma Inc 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
- LIDOCAINE
- Manufacturer
- Shinpharma Inc
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 69903-003
- Application
- M016
- Label effective
- 20260430
About this product
Dr. Numb is an FDA-registered drug product whose active ingredient is LIDOCAINE. It is labelled by Shinpharma Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 69903-003, application M016, label effective 20260430. It is one of 152 FDA drug label records sharing the active ingredient LIDOCAINE. 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 are most often described in connection with: temporarily relieves, itching due, insect bites, minor burns, 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 due to insect bites minor burns minor cuts minor scrapes minor skin irritations sunburn
Dosage & Administration
Directions Adults and children 2 years and older: Apply externally to the affected area up to 3 to 4 times a day Children under 2 years: Consult a doctor
Warnings
Warnings For external use only When using this product avoid contact with the eyes do not use in large quantities, particularly over raw surfaces or blistered areas Stop the use and consult doctor if allergic reaction occurs condition worsens or does not improve within 7 days symptoms clear up and return within a few days redness, irritation, swelling, pain or other symptoms begin or increase KEEP OUR 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 compare
FDA lists 152 drug label records with LIDOCAINE 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 |
|---|---|---|---|
| — | — | Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. | 10 |
| — | — | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 9 |
| — | — | Proficient Rx LP | 6 |
| — | — | Bryant Ranch Prepack | 5 |
| — | — | Preferred Pharmaceuticals Inc. | 5 |
Frequently asked questions
What is Dr. Numb used for?
Uses Temporarily relieves pain and itching due to insect bites minor burns minor cuts minor scrapes minor skin irritations sunburn
Who makes Dr. Numb?
Shinpharma Inc is the labeler of record for Dr. Numb. 152 FDA label records share the active ingredient LIDOCAINE, 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 Dr. Numb 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 Dr. Numb 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?
Yes. 152 FDA drug label records list LIDOCAINE 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 Dr. Numb 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.