FDA.reportPublic FDA data

5% Dr.care Numb cream

Manufacturer
Shengnan (Guangzhou) Cosmetics Co., LTD
Effective date
2025-03-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:56:43

Label at a glance#

Product5% Dr.care Numb cream
Active ingredientLIDOCAINE
Label structure9 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

For external use only.Stop use and consulta doctor if an allergicreaction occurs.
Keep out of reach of children. Keep away from direct sunlight and store at a temperature between 15 to 30'C(59 to 86'F).

OTC - PURPOSE SECTION

Best for painless tattoo and cosmetic procedures

OTC - STOP USE SECTION

Discontinueuse if signs of irritation or rash occur

OTC - ACTIVE INGREDIENT SECTION

5% Lidocaine

OTC - WHEN USING SECTION

Wash the area with soap and water.

INACTIVE INGREDIENT SECTION

Water, Aleo vera
extract, Vitamin E,Propylene Glycol,Carbomer, Glycerin,Disodium Edta.
Hydroxyacetophenone,
1.2-Hexanediol, Mentha Arvensis Leaf Extract,
Chrysanthellum
Indicum Extract,
Portulaca Oleracea Extract.

DOSAGE & ADMINISTRATION SECTION

Apply 1-3 times a week

INDICATIONS & USAGE SECTION

Apply a 2mm thick layer of cream, rub it in, and cover it with a waterproof film.Leave on for approximately 90 minutes before your procedure for maximum numbing effect.

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84019-028-015% Dr.care Numb cream30 g in 1 BOTTLECREAM301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84019-0285% DR.CARE NUMB CREAM (LIDOCAINE) CREAM [SHENGNAN (GUANGZHOU) COSMETICS CO., LTD]1Current NDC, 1 package rows20250308_2f905d76-ef9c-c844-e063-6394a90a4dc9.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84019-02884019-028-01

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
GLYCERINPDC6A3C0OXIACT
CARBOMER0A5MM307FCIACT
WATER059QF0KO0RIACT
LIDOCAINE98PI200987ACTIB

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
5% Dr.care Numb creamLIDOCAINEShengnan (Guangzhou) Cosmetics Co., LTD2f905d76-ef9c-c844-e063-6394a90a4dc92025-03-04WarningsExact identifier
ndc (package): 84019-028-01
ndc (product): 84019-028
ndc11 (package): 84019002801
spl id: 2f905d76-ef9d-c844-e063-6394a90a4dc9
spl set id: 2f905d76-ef9c-c844-e063-6394a90a4dc9

Reported adverse events (FAERS/openFDA)#

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