PROINNATE NUMBING CREAM- menthol cream

PROINNATE Numbing Cream by

Drug Labeling and Warnings

PROINNATE Numbing Cream by is a Otc medication manufactured, distributed, or labeled by Guangzhou Haishi Biological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Menthol 10%

Purpose

For the temporary relief ofpain and itching associated withminor burns, sunburn, minorcuts, scrapes, and insect bites.

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 longergives better effects).5.Remove any remaining creamand wait an additional 5 minutesfor the numbing sensation toreach its peak.

Warnings

For extemal use only

Stop Use

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

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

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

Keep Out Of Reach Of Children

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

Inactive ingredients

Aqua 74.5%
Ethylhexyl Palmitate 3%
Glycerin 5%
Propylene Glycol 5%
DaphneFeddei Extract 2%
Paeonol 0.5%

Dosage & administration

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROINNATE NUMBING CREAM 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60771-0039
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DAPHNETIN (UNII: XC84571RD2)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
GLYCERIN (UNII: PDC6A3C0OX)
AQUA (UNII: 059QF0KO0R)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
PAEONOL (UNII: 3R834EPI82)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60771-0039-1	30 g in 1 JAR; Type 0: Not a Combination Product	10/10/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	10/10/2025

Labeler - Guangzhou Haishi Biological Technology Co., Ltd. (421262738)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Haishi Biological Technology Co., Ltd.		421262738	manufacture(60771-0039)