VBBV Numbing

LIDOCAINE TOPICAL HUMAN OTC DRUG

VBBV Numbing is an FDA drug label for the active ingredient LIDOCAINE manufactured by Jiashen International Trade Limited 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 20260720.

Generic name
LIDOCAINE
Manufacturer
Jiashen International Trade Limited
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
84867-015
Application
M017
Label effective
20260720

About this product

VBBV Numbing is an FDA-registered drug product whose active ingredient is LIDOCAINE. It is labelled by Jiashen International Trade Limited taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 84867-015, application M017, label effective 20260720. 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: directions children, years age, consult physician. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

LIDOCAINE 4%

Indications & Usage

Directions: Children under 12 years of age: Consult a physician.

Dosage & Administration

Adults:1. When practical, cleanse the affected area with mild soap and warmwater and rinse thoroughly. Gently dry it by patting or blotting it withtoilet tissue or a soft cloth before applying this product. 2. Apply a thin layer to the affected area every 6 to 8 hours, not toexceed 3 applications in a 24-hour period.

Warnings

Warnings:For external use onlyAvoid contact with the eyes.Do not use in large quantities, particularly over raw surfaces or blistered areas anddo not exceed the recommended daily dosage unless directed by a doctor. Close ASK DOCTOR Ask a doctor before use if you havelf pregnant or breast-feeding, ask a health professional before use. Close STOP USE Stop use and ask a doctor if lf symptoms of redness or allergy occur, discontinue use, and consult a physician.

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How 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 formProductsManufacturerProducts
— — 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 VBBV Numbing used for?
Directions: Children under 12 years of age: Consult a physician.

Who makes VBBV Numbing?
Jiashen International Trade Limited is the labeler of record for VBBV Numbing. 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 VBBV Numbing 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 VBBV Numbing 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 VBBV Numbing 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.