LEKON PAIN RELIEF OIL- l-menthol oil

Lekon Pain Relief Oil by

Drug Labeling and Warnings

Lekon Pain Relief Oil by is a Otc medication manufactured, distributed, or labeled by CAI Industries Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Menthol 5%

Purpose

External analgesic

Uses

Temporarily relieves muscle and joint pains: backaches, arthritis, strains, bruises, sprains

Warnings

For external use only

When using this product 

• avoid contact with the eyes or mucous membranes 
• do not use on wounds or broken skin

Stop use and ask a doctor if

• conditions worsen 
• excessive skin irritation develops
• nausea, vomiting, abdominal discomfort, diarrhea, or a skin rash occurs
• symptoms persists for more than 7 days

If pregnant or breast-feeding, ask a doctor before use.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

Directions

• Adults and children 12 years of age and older: apply few drops into palm or hand nad massage into affected areas 
• Children under 12 years of age: consult your physician

Inactive ingredients

CLEMATIS TERNIFLORA VAR. MANDSHURICA ROOT, MOMORDICA COCHINCHINENSIS SEED, RICINUS COMMUNIS SEED, MYRRH, FRANKINCENSE, METHYL SALICYLATE

Product label

INGREDIENTS AND APPEARANCE

LEKON PAIN RELIEF OIL 
l-menthol oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85954-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7)	LEVOMENTHOL	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CLEMATIS TERNIFLORA VAR. MANDSHURICA ROOT (UNII: 33SL879G6T)
MOMORDICA COCHINCHINENSIS SEED (UNII: 2T87O1UPVD)
RICINUS COMMUNIS SEED (UNII: 7EK4SFN1TX)
MYRRH (UNII: JC71GJ1F3L)
FRANKINCENSE (UNII: R9XLF1R1WM)
METHYL SALICYLATE (UNII: LAV5U5022Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85954-001-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/23/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/23/2025

Labeler - CAI Industries Corp. (859060303)