4% Menthol PAIN RELIEF GEL

Manufacturer
Universal Distribution Center LLC
Effective date
2026-01-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:34:38

Label at a glance#

Product4% Menthol PAIN RELIEF
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure9 sections

Indications and uses

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

Dosage and administration

• 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

Storage and handling

Store at room temperature • Protect from direct sunlight.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 4%

Purpose

OTC - PURPOSE SECTION

Pain Relief Gel

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

• 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

STORAGE AND HANDLING SECTION

Store at room temperature • Protect from direct sunlight.

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

4% MENTHOL PAIN RELIEF4% MENTHOL PAIN RELIEF

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
415974menthol 4 % Topical GelPSN1
415974menthol 0.04 MG/MG Topical GelSCD1
415974menthol 4 % Topical GelSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52000-439-254% Menthol PAIN RELIEF74 mL in 1 BOTTLEGEL741

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52000-43952000-439-25

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4% Menthol PAIN RELIEFMENTHOLUniversal Distribution Center LLC7fb95135-4151-4ef4-bb6d-75251cafff6c2026-01-09WarningsExact identifier
ndc (package): 52000-439-25
ndc (product): 52000-439
ndc11 (package): 52000043925
spl id: 8beb3f46-515f-4b8d-ad05-06be2df6ca08
spl set id: 7fb95135-4151-4ef4-bb6d-75251cafff6c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.