PUVIDA NUMBING

Manufacturer
Jiangxi Yudexi Pharmaceutical Co., LTD | Jiangxi Zhongletang Pharmaceuticals Co.,Ltd.
Effective date
2026-03-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-06-03 17:58:59

Label at a glance#

ProductPUVIDA NUMBING
Active ingredientLIDOCAINE
Label structure13 sections

Dosage and administration

·Before applying the numbing cream, make sure to wash your hands thoroughly and put on disposable procedure gloves. ·Clean the area of the body receiving the procedure. Dry completely. ·Apply a generous amount of numbing cream to the cleaned area and rub it in thoroughly in a circular motion for 30 to 60 seconds. Then, cover with plastic wrap. ·Leave the cream and wrap in place for 30 to 45 minutes. Wipe away the ...

Storage and handling

Store between 15‑30°C (59‑86°F). Avoid freezing and excessive heat above 40°C (104°F).

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4% (w/w)

Purpose

OTC - PURPOSE SECTION

External analgesic

Use

INDICATIONS & USAGE SECTION

For temporary relief of local discomfort, itching, pain, soreness, or burning associated with minor skin procedures.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

·In children under 2 years of age or on irritated or sensitive skin
·Do not exceed the recommended daily dosage unless directed by a doctor.
·Avoid contact with eyes. If this happens, rinse thoroughly with water.
·If symptoms persist for more than 7 days or subside but occur again within 3 days, stop use and consult a physician.

When Using

OTC - WHEN USING SECTION

·Avoid contact with eyes, lf this happens, rinse thoroughly with water.

Stop Use

OTC - STOP USE SECTION

Stop use and seek medical attention if signs of an allergy occur, such as redness, irritation, swelling, pain, or other severe symptoms. If symptoms do not subside completely within 7 days, seek medical help.

Ask Doctor

OTC - ASK DOCTOR SECTION

Stop use and seek medical attention if signs of an allergy occur, such as redness, irritation, swelling, pain, or other severe symptoms. If symptoms do not subside completely within 7 days, seek medical help.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

·Before applying the numbing cream, make sure to wash your hands thoroughly and put on disposable procedure gloves.
·Clean the area of the body receiving the procedure. Dry completely.
·Apply a generous amount of numbing cream to the cleaned area and rub it in thoroughly in a circular motion for 30 to 60 seconds. Then, cover with plastic wrap.
·Leave the cream and wrap in place for 30 to 45 minutes. Wipe away the cream and thoroughly clean the area to prepare for the upcoming procedure.

Other information

STORAGE AND HANDLING SECTION

Store between 15‑30°C (59‑86°F). Avoid freezing and excessive heat above 40°C (104°F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Carbomer 934, Propylene Glycol, Soybean Lecithin, Alpha-Tocopherol Acetate, Benzyl Alcohol.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

44

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136979843981521GTIN-13: 6979843981521
EAN-13: 6979843981521
GTIN storage (14 digits): 06979843981521
278a1f8cc1c549f45958a4a34d2c9fd3.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85248-17385248-173-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
52d8125a-a334-67d6-e063-6294a90aa3d94de59570-6870-0592-e063-6294a90add872026-05-27WarningsExact identifier
spl set id: 4de59570-6870-0592-e063-6294a90add87

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.