PROINNATE Numbing Cream

Manufacturer
Guangdong Aimu Biological Technology Co., Ltd
Effective date
2025-12-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:28:06

Label at a glance#

ProductPROINNATE Numbing Cream
Active ingredientLIDOCAINE, MENTHOL
Label structure11 sections

Indications and uses

1.Before use, do a patch test toensure it suits your skin andnumbs effecitively. 2.Clean your hands andtreatment area thoroughly withmild soap and warm water. Drythem afterward. 3.Apply a THICK layer ofnumbing cream to the treatmentarea, making sure to cover boththe tattooed area and itssurroundings. 4.Wrap the area securely withplastic wrap and leave it on for40-50 minutes for the bestresults (keeping it on longe...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%
Menthol 6%

Purpose

OTC - PURPOSE SECTION

For the temporary relief of pain and itching associated with minor burns, sunburn, minorcuts, scrapes, and insect bites.

Uses

INDICATIONS & USAGE SECTION

1.Before use, do a patch test toensure it suits your skin andnumbs effecitively.
2.Clean your hands andtreatment area thoroughly withmild soap and warm water. Drythem afterward.
3.Apply a THICK layer ofnumbing cream to the treatmentarea, making sure to cover boththe tattooed area and itssurroundings.

4.Wrap the area securely withplastic wrap and leave it on for40-50 minutes for the bestresults (keeping it on longergives better effects).

5.Remove any remaining creamand wait an additional 5 minutes for the numbing sensation toreach its peak.

Warnings

WARNINGS SECTION

For extemal use only

Stop Use

OTC - STOP USE SECTION

Stop and ask a doctor if-an allergic reaction occurs.-symptom do not improve or ifredness, irritation, swelling. painor other symptoms develop orincrease.

Do Not Use

OTC - DO NOT USE SECTION

Do not exceed the recommendeddaily dosage unless directed by adoctor. Avoid contact with theeyes. Do not use if you areallergic to the ingredients in thisproduct or if the seal is brokenor missing

When Using

OTC - WHEN USING SECTION

If pregnant or breast-feeding,ask a health professional beforeuse.

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out ofreach of children. incase of accidental ingestion,seek medical advice immediatelyor contact a Poison ControlCenter right away.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Ethylhexyl Palmitate 12%
Glycerin 5%
Propylene Glycol 5%
Daphne Feddei Extract 0.5%
Aqua 67%
Paeonol 0.5%

Dosage & administration

DOSAGE & ADMINISTRATION SECTION

Apply a THiCK layer ofnumbing cream to the treatmentarea, making sure to cover boththe tattooed area and its surroundings

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label.Label.

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2729431lidocaine 4 % / menthol 6 % Topical CreamPSN1
2729431lidocaine 40 MG/ML / menthol 60 MG/ML Topical CreamSCD1
2729431lidocaine 4 % / menthol 6 % Topical CreamSY1

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
83566-562-01PROINNATE Numbing Cream30 g in 1 BOXCREAM301

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-56283566-562-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
PROINNATE Numbing CreamLIDOCAINE,MENTHOLGuangdong Aimu Biological Technology Co., Ltd46895ddb-0b9f-675e-e063-6394a90adf232025-12-22WarningsExact identifier
ndc (package): 83566-562-01
ndc (product): 83566-562
ndc11 (package): 83566056201
spl id: 46895ddb-0ba0-675e-e063-6394a90adf23
spl set id: 46895ddb-0b9f-675e-e063-6394a90adf23

Reported adverse events (FAERS/openFDA)#

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