BonicaEaseX Menthol Pain Relieving Gel

Manufacturer: Planet (Anhui) Pharmaceutical Co.,Ltd
Effective date: 2026-04-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:53:32

Label at a glance#

ProductBonicaEaseX Menthol Pain Relieving

Active ingredientMENTHOL, UNSPECIFIED FORM

Label structure8 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints associated with: simple backache, arthritis, strains, bruises, and sprain.

Dosage and administration

Rub a thin film over the affected area not more than 3 to 4 times daily. Wash hands after use.

Contacts and useful links#

PhoneLabel contact1-816-716-0852

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 4%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints associated with: simple backache, arthritis, strains, bruises, and sprain.

Warnings

WARNINGS SECTION

• Please read all directions and warnings as follows and use only as directed. For external use only. • Flammable: Keep away from excessive heat or open flame. Do not heat, microwave, add to hot water or any container where heating water may cause splattering and result in burns. • If pregnant or breast-feeding, ask a health professional before use. • Do not bandage tightly. • Avoid contact with the eyes. • Do not apply to wounds or damaged skin

Keep out of reach of children and pets.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Do not use

OTC - DO NOT USE SECTION

• Alone if you are under the age of 12, please consult a doctor. • If you’re allergic to the listed ingredients. • If the package arrives damaged or opened. • at the same time as other topical analgesics. • on mucous membranes, cuts, broken, swollen, or irritated skin.

Stop use and ask a doctor if

OTC - STOP USE SECTION

• if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. • if you experience any signs of deterioration or skin injury, such as redness, irritation, swelling, or blistering. • if the arthritic pain persists for more than 10 days, or redness is presen

Directions

DOSAGE & ADMINISTRATION SECTION

Rub a thin film over the affected area not more than 3 to 4 times daily.
Wash hands after use.

Other information

SPL UNCLASSIFIED SECTION

Store it in a dry place at room temperature between 20–25 °C (68–77 °F) and away from direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

• Arnica Oil • Calendula Oil • Carbomer • Dimethyl Isosorbide • Glycerin • Isopropyl Alcohol • Lemon Oil • Triethanolamine • Tea Tree Oil • Water

Questions and Comments?

OTC - QUESTIONS SECTION

1-816-716-0852 Monday-Friday 9AM-5PM

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Outer Package04Inner Package04

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
415974	menthol 4 % Topical Gel	PSN	1
415974	menthol 0.04 MG/MG Topical Gel	SCD	1
415974	menthol 4 % Topical Gel	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75568-043-00	BonicaEaseX Menthol Pain Relieving	3 in 1 BOX	GEL	3		1
75568-043-00	BonicaEaseX Menthol Pain Relieving	118 mL in 1 TUBE	GEL	118		1

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

BonicaEaseX Menthol Pain Relieving
MENTHOL, UNSPECIFIED FORM
CALENDULA OFFICINALIS FLOWER
CARBOMER
DIMETHYL ISOSORBIDE
GLYCERIN
ISOPROPYL ALCOHOL
LEMON OIL
TRIETHANOLAMINE
TEA TREE OIL
WATER
MENTHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75568-043	75568-043-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CALENDULA OFFICINALIS FLOWER	P0M7O4Y7YD	IACT
CARBOMER	0A5MM307FC	IACT
DIMETHYL ISOSORBIDE	SA6A6V432S	IACT
GLYCERIN	PDC6A3C0OX	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
LEMON OIL	I9GRO824LL	IACT
TRIETHANOLAMINE	9O3K93S3TK	IACT
TEA TREE OIL	VIF565UC2G	IACT
WATER	059QF0KO0R	IACT
MENTHOL, UNSPECIFIED FORM	L7T10EIP3A	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
BonicaEaseX Menthol Pain Relieving	MENTHOL, UNSPECIFIED FORM	Planet (Anhui) Pharmaceutical Co.,Ltd	4d84b4fb-8f55-4b2b-b261-858edb7f3144	2026-04-10	Warnings	Exact identifier ndc (package): 75568-043-00 ndc (product): 75568-043 ndc11 (package): 75568004300 spl id: 4f1bd117-096a-4915-e063-6394a90a8a43 spl set id: 4d84b4fb-8f55-4b2b-b261-858edb7f3144

Reported adverse events (FAERS/openFDA)#

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