FDA.reportPublic FDA data

4% 10gTATTOO Numb Cream

Manufacturer
Shengnan (Guangzhou) Cosmetics Co., LTD
Effective date
2025-04-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:58:44

Label at a glance#

Product4% 10gTATTOO Numb Cream
Active ingredientLIDOCAINE
Label structure9 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

For external use only.Avoid contact with eyes.Patch test before full use.Patch test before full use.

OTC - PURPOSE SECTION

For numbing a localized topical area to ease painduring tattooing and cosmetic procedures.

OTC - STOP USE SECTION

Discontinue use if irritation occurs.

OTC - ACTIVE INGREDIENT SECTION

4% LIDOCAINE

OTC - WHEN USING SECTION

Wash the area with soap. Apply a 2 mm-thick layer, rub it in for 1-2 minutes, and
cover with a waterproof film approximately 30-50 minutes before your procedure.

INACTIVE INGREDIENT SECTION

Benzyl Alcohol, Carbomer, Lecithin,Mentha Arvensis Leaf Extract,chrysanthemum indicum Extract, Portulaca Oleracea Extract,Propylene Glycol, Tocopheryl Acetate, Water

DOSAGE & ADMINISTRATION SECTION

Apply 1-3 times a week

INDICATIONS & USAGE SECTION

Store in a cool place at 59-68°F, away from direct sunlight.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84019-031-014% 10gTATTOO Numb Cream10 g in 1 BOTTLECREAM101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84019-0314% 10GTATTOO NUMB CREAM (4% LIDOCAINE) CREAM [SHENGNAN (GUANGZHOU) COSMETICS CO., LTD]1Current NDC, 1 package rows20250409_322daa32-a74e-1fee-e063-6294a90a37aa.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84019-03184019-031-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER0A5MM307FCIACT
WATER059QF0KO0RIACT
LIDOCAINE98PI200987ACTIB
BENZYL ALCOHOLLKG8494WBHIACT

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
4% 10gTATTOO Numb Cream4% LIDOCAINEShengnan (Guangzhou) Cosmetics Co., LTD322daa32-a74e-1fee-e063-6294a90a37aa2025-04-07WarningsExact identifier
ndc (package): 84019-031-01
ndc (product): 84019-031
ndc11 (package): 84019003101
spl id: 322daa32-a74f-1fee-e063-6294a90a37aa
spl set id: 322daa32-a74e-1fee-e063-6294a90a37aa

Reported adverse events (FAERS/openFDA)#

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