BONICAEASEX 24 HOUR MENTHOL PAIN RELIEVING- menthol, unspecified form patch

Drug Labeling and Warnings

Drug Details [pdf]

Drug Facts

Active Ingredient

Menthol 5%

Purpose

Topical Analgesic

Use

Temporarily relieves minor aches and pains of muscles and joints due to

Arthritis Simple backache  Strains  Sprains  Bruises

Warnings

For external use only

Do not use

On wounds or damaged skin  With a heating pad

If you are allergic to any ingredients of this product

When using this product

• Use only as directed
• Avoid contact with the eyes, mucous membranes, or rashes

Stop use and ask a doctor if

Excessive redness or irritation is present

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

If pregnant or breast-feeding,

ask a health professional before use.

Keep out of reach of children.

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

Directions

• Adults and children 12 years of age and over:
  • Clean and dry affected area
  • Remove film from patch and apply to the skin
  • Use one patch for up to 24 hours
• Children under 12 years of age: Consult a doctor

Other information

• Avoid storing product in direct sunlight
• Protect product from excessive moisture

Inactive Ingredients

castor oil, dihydroxyaluminum aminoacetate, disodium edeta dihydrate, glycerol, isopropyl myristate, polyacrylic acid(250000 MW), polysorbate 80, polyvinyl alcohol, propylene glycol, silicon dioxide, sodium polyacrylate, tartaric acid, titanium dioxide, urea, water

Questions and Comments?

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

Package Labeling:

INGREDIENTS AND APPEARANCE

BONICAEASEX 24 HOUR MENTHOL PAIN RELIEVING 
menthol, unspecified form patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 75568-045
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	50 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CASTOR OIL (UNII: D5340Y2I9G)
DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TARTARIC ACID (UNII: W4888I119H)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
UREA (UNII: 8W8T17847W)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 75568-045-00	3 in 1 BOX	04/15/2026
1		5 in 1 POUCH
1		9.1 g in 1 PATCH; 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 - Planet (Anhui) Pharmaceutical Co., Ltd. (618456104)

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