TUIWARO NUMBING CREAM- numbing cream cream

Drug Labeling and Warnings

Drug Details [pdf]

Active Ingredient

5% Menthol

Ask a doctore before use

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

Keep Out Of Reach Of Children

If swallowed, get medical help.

Purpose

Topical Analgesic

Stop Use

Do not get into eyes
Do not exceed recommended dosage

When Using

Avoid contact with eyes.

Inactive ingredients

Tocopheryl Acetate

Emu Oil

Propylene Glycol

Arnica

Glycerin

Aesculus Hippocastanum (Horse Chestnut) Extract

Lecithin (Soybean)

Curcuma Longa Extract (Turmeric Extract)

Aqua (Water)

Directions

■ When practical, clean the area with mild soap and warm water and rinse thoroughly.
■ Gently dry by patting or blotting with toilet tissue or a soft cloth before applying.
■ Adults and children 12 years and older: apply externally to the affected area up to 4 times a day.
■ Children under 12 years of age: consult a doctor.
■ To use finger cots: roll one finger cot over the finger. Gently squeeze cream onto the finger cot. Smooth a layer of the cream.

Warnings

For external use only.

Uses

For the temporary relief of localized pain, itching, or discomfort from minor skin irritations.

Do Not Use

Do not use on wounds or damaged skin

PRINCIPAL DISPLAY PANEL

Brand: tuiwaro

Name: Analgesic Cream

Size: 1.75 OZ / 50 g

INGREDIENTS AND APPEARANCE

TUIWARO NUMBING CREAM 
numbing cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87408-012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
EMU OIL (UNII: 344821WD61)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ARNICA MONTANA (UNII: O80TY208ZW)
GLYCERIN (UNII: PDC6A3C0OX)
HORSE CHESTNUT (UNII: 3C18L6RJAZ)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
CURCUMA LONGA (TURMERIC) ROOT POWDER (UNII: 856YO1Z64F)
AQUA (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87408-012-01	1 in 1 CARTON	04/15/2026
1		50 g in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/15/2026

Labeler - Guangzhou Jingliang Cosmetics Co., Ltd. (515462936)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Jingliang Cosmetics Co., Ltd.		515462936	manufacture(87408-012)