PROINNATE Numbing Cream

Manufacturer
Guangzhou Haishi Biological Technology Co., Ltd.
Effective date
2025-10-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:38:47

Label at a glance#

ProductPROINNATE Numbing Cream
Active ingredientMENTHOL
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 longer...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Purpose

OTC - PURPOSE SECTION

For the temporary relief ofpain and itching associated withminor 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 minutesfor 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

Aqua 74.5%
Ethylhexyl Palmitate 3%
Glycerin 5%
Propylene Glycol 5%
DaphneFeddei Extract 2%
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 itssurroundings

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label.Label.

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
253020menthol 10 % Topical CreamPSN1
253020menthol 100 MG/ML Topical CreamSCD1
253020menthol 10 % Topical CreamSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60771-0039-1PROINNATE Numbing Cream30 g in 1 JARCREAM301

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60771-003960771-0039-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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 CreamMENTHOLGuangzhou Haishi Biological Technology Co., Ltd.40c63645-8ed3-82b3-e063-6294a90a52672025-10-13WarningsExact identifier
ndc (package): 60771-0039-1
ndc (product): 60771-0039
ndc11 (package): 60771003901
spl id: 40c63645-8ed4-82b3-e063-6294a90a5267
spl set id: 40c63645-8ed3-82b3-e063-6294a90a5267

Reported adverse events (FAERS/openFDA)#

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