BONICAEASEX MENTHOL PAIN RELIEVING- menthol, unspecified form gel

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active Ingredient

Menthol 4%

Purpose

Topical Analgesic

Uses

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

Warnings

 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.

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

Do not use

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

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

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

Other information

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

Inactive ingredients

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

Questions and Comments?

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

Package Labeling:

INGREDIENTS AND APPEARANCE

BONICAEASEX MENTHOL PAIN RELIEVING 
menthol, unspecified form gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75568-043
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	40 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
CARBOMER (UNII: 0A5MM307FC)
DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
LEMON OIL (UNII: I9GRO824LL)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
TEA TREE OIL (UNII: VIF565UC2G)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75568-043-00	3 in 1 BOX	03/31/2026
1		118 mL in 1 TUBE; 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	03/31/2026

Labeler - Planet (Anhui) Pharmaceutical Co.,Ltd (618456104)

Registrant - Planet (Anhui) Pharmaceutical Co.,Ltd (618456104)