4% MENTHOL PAIN RELIEF- menthol gel

4% Menthol PAIN RELIEF by

Drug Labeling and Warnings

4% Menthol PAIN RELIEF by is a Otc medication manufactured, distributed, or labeled by Universal Distribution Center LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug facts

Active ingredient

Menthol 4%

Purpose

Pain Relief Gel

Uses

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

Warnings

For external use only.

Flammable: Keep away from excessive heat or open flame

When using this product  use only as directed avoid contact with the eyes or on mucous membranes do not apply to wounds or damaged skin  do not apply to irritated skin or if excessive irritation develops  do not bandage tightly or use with heating pad or device

Stop use and ask a doctor if ​ you experience pain, swelling or blistering of the skin condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days arthritic pain persists for more than 10 days, or redness is present, or in conditions affecting children under 12 years of age

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 older: rub a thin film over affected area not more than3 to 4 times daily  children under 12 years of age: consult a physician  wash hands after use with cool water

Other information

Store at room temperature  Protect from direct sunlight.

Inactive ingredients

Aloe Barbadensis Leaf Juice, Arctium Lappa Extract, Arnica Montana Flower Extract, Aminomethyl Propanol, Boswellia Serrata Extract, Butylene Glycol, Calendula Officinalis Flower Extract, Camellia Sinensis Leaf Extract, Camphor, Carbomer, FD&C Blue NO.1, FD&C Yellow No.5, Glycerin, Ilex Paraguariensis Leaf Extract, Isopropyl Alcohol, Isopropyl Myristate, Melissa Officinalis Leaf Extract, Methyl Methacrylate Crosspolymer, Tocopheryl Acetate, Water.

SPL UNCLASSIFIED SECTION

COOLING MENTHOL FORMULA

✓ Soothes sore muscles
✓ Relieves back, neck & joint pain
✓ Fast-absorbing & non-greasy

Mfd for and Distributed by:
Universal Distribution Center LLC
330 Applegarth Road, Monroe Township, NJ 08831

www.universaldc.com

MADE IN CHINA

Packaging

INGREDIENTS AND APPEARANCE

4% MENTHOL PAIN RELIEF 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-439
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	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
ARCTIUM LAPPA WHOLE (UNII: 73070DU1LA)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
CAMPHOR (NATURAL) (UNII: N20HL7Q941)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
GLYCERIN (UNII: PDC6A3C0OX)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-439-25	74 mL in 1 BOTTLE; Type 0: Not a Combination Product	01/19/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	01/19/2026

Labeler - Universal Distribution Center LLC (019180459)