tuiwaro Numbing Cream
tuiwaro Numbing Cream is an FDA drug label for the active ingredient NUMBING CREAM manufactured by Guangzhou Jingliang Cosmetics Co., Ltd. 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 20260414.
- Generic name
- NUMBING CREAM
- Manufacturer
- Guangzhou Jingliang Cosmetics Co., Ltd.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87408-012
- Application
- M017
- Label effective
- 20260414
About this product
tuiwaro Numbing Cream is an FDA-registered drug product whose active ingredient is NUMBING CREAM. It is labelled by Guangzhou Jingliang Cosmetics Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87408-012, application M017, label effective 20260414. It is one of 5 FDA drug label records sharing the active ingredient NUMBING CREAM. 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 NUMBING CREAM are most often described in connection with: temporary relief, localized pain, itching discomfort, minor skin. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses For the temporary relief of localized pain, itching, or discomfort from minor skin irritations.
Dosage & Administration
Directions ■ When practical, clean the area with mild soap and warm water and rinse thoroughly. ■ Gently dry by patting or blotting with toilet tissue or a soft cloth before applying. ■ Adults and children 12 years and older: apply externally to the affected area up to 4 times a day. ■ Children under 12 years of age: consult a doctor. ■ To use finger cots: roll one finger cot over the finger. Gently squeeze cream onto the finger cot. Smooth a layer of the cream.
Warnings
Warnings For external use only.
More products with the same ingredient
NUMBING CREAMArlun Numbing Cream
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View labelMUYOHON Numbing Cream
View labelHow products containing NUMBING CREAM compare
FDA lists 5 drug label records with NUMBING CREAM 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 Jingliang Cosmetics Co., Ltd. | 5 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is tuiwaro Numbing Cream used for?
Uses For the temporary relief of localized pain, itching, or discomfort from minor skin irritations.
Who makes tuiwaro Numbing Cream?
Guangzhou Jingliang Cosmetics Co., Ltd. is the labeler of record for tuiwaro Numbing Cream. 5 FDA label records share the active ingredient NUMBING CREAM, 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 tuiwaro Numbing Cream 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 tuiwaro Numbing Cream 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 NUMBING CREAM?
Yes. 5 FDA drug label records list NUMBING CREAM 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 tuiwaro Numbing Cream 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.