FDA.reportPublic FDA data

Nupharmisto Tattoo Numbing Cream

Manufacturer
Orange Lab, Inc
Effective date
2024-05-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:11:48

Label at a glance#

ProductNupharmisto Tattoo Numbing Cream
Active ingredientLIDOCAINE
Label structure15 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active IngredientActive Ingredient

ask doctor

OTC - ASK DOCTOR SECTION

ask doctorask doctor

OTC - DO NOT USE SECTION

do not usedo not use

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of childrenkeep out of reach of children

OTC - PREGNANCY OR BREAST FEEDING SECTION

if pregnantif pregnant

Purpose

OTC - PURPOSE SECTION

purposepurpose

questions

OTC - QUESTIONS SECTION

questionsquestions

Stop use warnings

OTC - STOP USE SECTION

warningswarnings

When using

OTC - WHEN USING SECTION

directionsdirections

Directions

DOSAGE & ADMINISTRATION SECTION

directionsdirections

warnings sections

WARNINGS SECTION

warningwarning

Active Ingredients

INACTIVE INGREDIENT SECTION

inactive ingredientsinactive ingredients

How to use it correctly

INDICATIONS & USAGE SECTION

how to use correctlyhow to use correctly

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

bottle label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottle labelbottle label

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
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71331-115-042026-01-29C16284748780-149896155-a8e8-586f-e063-e6dba90add90Nupharmisto Lidocaine Tattoo Numbing Cream 4%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71331-115-04Nupharmisto Tattoo Numbing Cream50 g in 1 PACKAGECREAM502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71331-115NUPHARMISTO TATTOO NUMBING CREAM (LIDOCAINE) CREAM [ORANGE LAB, INC]21 package rows20240501_14d28254-8633-253e-e063-6294a90a0f9b.zip

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71331-11571331-115-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S)8Z5ZAL5H3VIACT
ETHYLHEXYL PALMITATE2865993309IACT
HYDROGENATED POLYDECENE (1500 CST)4YI0729529IACT
SODIUM POLYACRYLATE (8000 MW)285CYO341LIACT
ALLANTOIN344S277G0ZIACT
TRIDECETH-63T5PCR2H0CIACT
EMU OIL344821WD61IACT
PHENOXYETHANOLHIE492ZZ3TIACT
EDETATE SODIUM TETRAHYDRATEL13NHD21X6IACT
DIMETHYL ISOSORBIDESA6A6V432SIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SUNFLOWER OIL3W1JG795YIIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
LIDOCAINE98PI200987ACTIB
ETHYLHEXYLGLYCERIN147D247K3PIACT
WATER059QF0KO0RIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT

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
150cc0f9-94a6-d750-e063-6394a90a160f14d28254-8633-253e-e063-6294a90a0f9b2024-05-01WarningsExact identifier
spl id: 150cc0f9-94a6-d750-e063-6394a90a160f
spl set id: 14d28254-8633-253e-e063-6294a90a0f9b

Reported adverse events (FAERS/openFDA)#

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