Numb Cream

Manufacturer
Shengnan (Guangzhou) Cosmetics Co., LTD
Effective date
2024-03-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:09:24

Label at a glance#

ProductNumb Cream
Active ingredientLIDOCAINE
Label structure12 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Numb Cream

OTC - ACTIVE INGREDIENT SECTION

LIDOCAINE 4%

OTC - PURPOSE SECTION

Topical Analgesic

INDICATIONS & USAGE SECTION

For temporarily relieve local discomfort, itching, pain, soreness or burning sensation on hands, legs, back and other skin.

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

lf pregnant or breast-feeding, ask a health professional before use.

OTC - WHEN USING SECTION

Use only as directed.
Avoid contact with the eyes,
mucous membranes, or rashes.
Do not bandage tightly.

OTC - STOP USE SECTION

skin reactions such as redness.swelling, blistering or other discomfort occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.
lf swallowed accidentally, get medical help or contact with Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

1.For optimum results cleanse the affected area with mild soap and warm water and rinse thoroughly.
2.Apply externally to the affected area up to 6 times.

INACTIVE INGREDIENT SECTION

Water
Propylene Glycol
Carbomer
Glycerin
Disodium Edta
Hydroxyacetophenone
1.2-Hexanediol
Mentha Arvensis Leaf Extract
Chrysanthellum Indicum Extract
Portulaca Oleracea Extract
Peg-40 Hydrogenated Castor Oil
Epinephrine
Tetracaine
Prilocaine
Borneol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1421893lidocaine 4 % Topical CreamPSN2
1421893lidocaine 40 MG/ML Topical CreamSCD2
1421893lidocaine 4 % Topical CreamSY2

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
0b4ec9ca-d305-43fc-88dd-7a510313efe0Product name120260105
bb209f42-a85f-4fee-9d3d-c9dded168625Product name120251208
49628fc7-2031-4c28-bd31-0ef3aa8f44a3Product name320251118
a26f29b9-6919-4f09-a354-491df8d2b97dProduct name120251021
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
cbf85893-59ef-423f-87d4-a573c000a8b9Product name820250731
b5b1095b-40cd-8a9e-b111-502545045b07Product name420250325
e190029e-423b-473c-8e04-2ada59b5b711Product name120250314
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
e0031c74-3853-42bc-8e10-86dbbe83992eProduct name220231116
f7046b89-2016-499a-adc6-78479172abc6Product name120230425
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
2686d634-e712-4007-8dbf-3d37c6c4d71fProduct name120181121
122d1fa8-7b9e-49b4-89ce-b062ffd1d947Product name120181030
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
bd49bb86-2d32-4a7a-a594-eeda2e29af42Product name120180118
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
3becbe78-12d9-4ad2-9b4c-1e36f8d1303aProduct name120170815
a993dfc5-f219-4460-bde6-30dd724d9ef0Product name120160818
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

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84019-301-01Numb Cream10 g in 1 TUBECREAM102
84019-301-01Numb Cream1 in 1 BOXCREAM12
84019-301-02Numb Cream1 in 1 BOXCREAM12
84019-301-02Numb Cream30 g in 1 TUBECREAM302
84019-301-03Numb Cream50 g in 1 TUBECREAM502
84019-301-03Numb Cream1 in 1 BOXCREAM12
84019-301-04Numb Cream1 in 1 BOXCREAM12
84019-301-04Numb Cream60 g in 1 TUBECREAM602
84019-301-05Numb Cream1 in 1 BOXCREAM12
84019-301-05Numb Cream100 g in 1 TUBECREAM1002
84019-301-06Numb Cream120 g in 1 TUBECREAM1202
84019-301-06Numb Cream1 in 1 BOXCREAM12
84019-301-07Numb Cream1 in 1 BOXCREAM12
84019-301-07Numb Cream150 g in 1 TUBECREAM1502
84019-301-08Numb Cream200 g in 1 TUBECREAM2002
84019-301-08Numb Cream1 in 1 BOXCREAM12
84019-301-09Numb Cream1 in 1 BOXCREAM12
84019-301-09Numb Cream250 g in 1 TUBECREAM2502
84019-301-10Numb Cream1 in 1 BOXCREAM12
84019-301-10Numb Cream300 g in 1 TUBECREAM3002
84019-301-11Numb Cream500 g in 1 TUBECREAM5002
84019-301-11Numb Cream1 in 1 BOXCREAM12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84019-301NUMB CREAM (LIDOCAINE) CREAM [SHENGNAN (GUANGZHOU) COSMETICS CO., LTD]222 package rows20240307_11f4bf92-0dbd-a83e-e063-6394a90a739a.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
12f87be4-d8c9-8c2f-e063-6294a90a1f5711f4bf92-0dbd-a83e-e063-6394a90a739a2024-03-06WarningsExact identifier
spl id: 12f87be4-d8c9-8c2f-e063-6294a90a1f57
spl set id: 11f4bf92-0dbd-a83e-e063-6394a90a739a

Reported adverse events (FAERS/openFDA)#

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