AUVON 4% MENTHOL PAIN RELIEF GEL- menthol gel

Auvon 4% Menthol Pain Relief Gel by

Drug Labeling and Warnings

Auvon 4% Menthol Pain Relief Gel by is a Otc medication manufactured, distributed, or labeled by SHENZHEN YUWEN E-COMMERCE CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Auvon 4% Menthol Pain Relief Gel

ACTIVE INGREDIENT

Menthol 4%

PURPOSE

Topical Analgestic

INDICATIONS & USAGE

Temporary relief from minor aches and paons of sore muscles and joints

WARNINGS

For external use only

DO NOT USE

If you are under 12 years of age

If you are allergic to the listed ingredients

If you are pregnent or breast feeding

On wounds, cuts, damaged/broken/irritated skin

WHEN USING

■ Use only as directed

■ Read and follow all directions and warnings on this label

STOP USE

You are experiencing pain, swelling or blistering

Redness is persent or irritation develops

Symptoms persist for more than 7 days or clear up and occur again within a few days

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

DOSAGE & ADMINISTRATION

Clean and dry the patch application area (no wound or hair), pull to separate the film, peel off one side of the film, apply the exposed patch to the skin, peel off the other side of the film, and press the patch firmly ■ Do not repeatedly use or repeatedly reapply the patch as far as possible

Use in te affected area no more than 4 times daily

Wash hands with cool water after use

STORAGE AND HANDLING

Store it in a dray place at a room temperature between 20-25°c and away from direct sunlight

INACTIVE INGREDIENT

Arctium Lappa (Burdock) Extract

Arnica Montana Flower Extract

Aloe Barbadensis Leaf Juice

Aminomethyl Propanol

Boswellia Serrata Extract

Camellia Sinensis(Green Tea) Leaf Extract

Camphor

Carbomer

Calendula Officinalis Flower Extract

FD&C Blue NO.1

FD&C Yellow No.5

Isopropyl Alcohol

Isopropyl Myristate,

Glycerin

Llex Paraguariensis Leaf Extract

Melissa Officinalis Leaf Extract

Methyl Methacrylate Crosspolymer

Tocopheryl Acetate

Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AUVON 4% MENTHOL PAIN RELIEF GEL 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83391-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7)	LEVOMENTHOL	0.04 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ARNICA MONTANA FLOWER WATER (UNII: U7L2JP51PR)
ALOE BARBADENSIS LEAF JUICE (UNII: ZY81Z83H0X)
CARBOMER (UNII: 0A5MM307FC)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
AMINOMETHYL PROPANOL (UNII: LU49E6626Q)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
WATER (UNII: 059QF0KO0R)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
BOSWELLIA SERRATA OIL (UNII: 5T1XCE6K8K)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
ARCTIUM LAPPA WHOLE (UNII: 73070DU1LA)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
CAMELLIA SINENSIS LEAF OIL (UNII: VC855RRT77)
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
GLYCERIN (UNII: PDC6A3C0OX)
MELISSA OFFICINALIS LEAF OIL (UNII: PTP6R7263M)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83391-007-01	89 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/08/2025
2	NDC: 83391-007-02	2 in 1 PACKAGE	02/08/2025
2	NDC: 83391-007-01	89 mL in 1 BOTTLE; Type 0: Not a Combination Product
3	NDC: 83391-007-03	3 in 1 PACKAGE	02/08/2025
3	NDC: 83391-007-01	89 mL 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	02/08/2025

Labeler - SHENZHEN YUWEN E-COMMERCE CO., LTD. (544559614)