2.5% MENTHOL PAIN RELIEF- menthol gel

2.5% Menthol PAIN RELIEF by

Drug Labeling and Warnings

2.5% 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 (in each gram)

Menthol 2.5%

Purpose

Topical analgesic

Uses

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

Warnings

For external use only.

Do not use
on wounds or damaged skin
with a heating pad
on a child under 12 years of age with arthritis-like conditions

Ask a doctor before use if you have redness over the affected area.

When using this product
avoid contact with eyes or mucous membranes
do not bandage tightly

Stop use and ask a doctor if  condition worsens or symptoms persist for more than 7 days  symptoms clear up and occur again within a few days  excessive skin irritation occurs

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

Directions

adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily children under 12 years of age: ask a doctor

Other information

store at 20° to 25°C (68° to 77°F)

Inactive ingredients

Cinnamomum camphora(camphor) bark oil, Carbomer, Ethylhexylglycerin, Glycerin, Isopropyl Alcohol, Methylparaben, Polysorbate 20, Propylparaben, Purified Water, Sodium Hydroxide.

SPL UNCLASSIFIED SECTION

COOLING MENTHOL FORMULA

✓ Relives back, neck & joint pain

✓ Fast-absorbing & non-greasy

Soothes sore muscles 

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

2.5% MENTHOL PAIN RELIEF 
menthol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52000-440
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	25 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
CAMPHOR OIL (UNII: 75IZZ8Y727)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
GLYCERIN (UNII: PDC6A3C0OX)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
METHYLPARABEN (UNII: A2I8C7HI9T)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52000-440-02	1 in 1 BOX	01/19/2026
1		57 g 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	01/19/2026

Labeler - Universal Distribution Center LLC (019180459)