MENTHOL by CHEMCO CORPORATIOM MENTHOL gel

MENTHOL by

Drug Labeling and Warnings

MENTHOL by is a Otc medication manufactured, distributed, or labeled by CHEMCO CORPORATIOM. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Menthol 4%

PURPOSE

Topical Analgesic

USE

Aid for temporary local relief of minor pain in muscles or joints.

WARNINGS

For external use only. · Ask a doctor before use if you have redness over affected area

WHEN USING

Use only as directed.
Do not bandage tightly or use with a heating pad.
Avoid contact with eyes and mucous membranes.
Do not apply to wounds or damaged, broken or irritated skin.
If you experience an allergic reaction, discontinue use and consult a doctor.

Do not expose the area treated with product to heat or direct sunlight.

STOP USE

Stop use and ask a doctor if

Condition worsens.
Redness is present.
Irritation develops.
Symptoms persist for more than 7 days or clear up occur again within a few days.

You experience signs injury, such as pain, swelling or blistering where the product was applied.

PREGNANCY 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 over 12 years

Apply a small amount to the affected area.
Massage in circular motion, let set for a few seconds.
Repeat as necessary, but no more than 3 to 4 times daily.

Children under 12 years of age: do not use, consult a doctor.

OTHER SAFETY INFORMATION

Store tightly closed in a dry place at controlled room temperature between 59°-86° F (15°-30° C).

INACTIVE INGREDIENT

Water (Aqua), Alcohol Denat, Ceteareth-25, Glycerin, Calendula Officinalis Extract, Caprylic/Capric Triglyceride, Carbomer, Sodium Hydroxide, Cannabis Sativa Seed Oil, Methyl Salicylate, Benzyl Alcohol, Salicylic Acid, Sorbic Acid.

PAIN RELIEF

INGREDIENTS AND APPEARANCE

MENTHOL 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49283-577
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A)	MENTHOL, UNSPECIFIED FORM	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CETEARETH-25 (UNII: 8FA93U5T67)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
GLYCERIN (UNII: PDC6A3C0OX)
ALCOHOL (UNII: 3K9958V90M)
SALICYLIC ACID (UNII: O414PZ4LPZ)
CARBOMER 940 (UNII: 4Q93RCW27E)
SORBIC ACID (UNII: X045WJ989B)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
METHYL SALICYLATE (UNII: LAV5U5022Y)
CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49283-577-03	90 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	12/20/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/20/2025

Labeler - CHEMCO CORPORATIOM (032495954)