Universal ARTHRITIS and SPORT

Manufacturer
Universal Distribution Center LLC
Effective date
2024-11-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:42:02

Label at a glance#

ProductUniversal ARTHRITIS and SPORT
Active ingredientMETHYL SALICYLATE, CAPSICUM
Label structure8 sections

Indications and uses

for the temporary relief of 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: apply to affected area not more than 3 to 4 times daily • Children under 12 years of age: ask a doctor

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate 0.61%

Capsicum 0.0012%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

for the temporary relief of minor aches and pains of muscles and joints associated with:

• simple backache  • arthritis • strains • bruises • sprains

Warnings

WARNINGS SECTION

For external use only

Do not use • other than as directed • on children under 12 years of age

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: apply to affected area not more than 3 to 4 times daily

• Children under 12 years of age: ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Camphor, FD & C Red No.40 (CI 16035), Isopropyl Alcohol, Magnesium Sulfate, Water (Aqua)

SPL UNCLASSIFIED SECTION

PENETRATING HEAT RUB

Formulated for:

Rubbing and Soaking

• Arthritis      • Aching Stiff Joints
• Aching Muscles  • Tired Aching Feet • Sprains

Extra Strength

with Rubbing Alcohol 

Distributed by:Universal Distribution Center LLC.
96 Distribution Boulevard, Edison,
NJ 08817

www.universaldc.com

Made in Jordan

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5200030352000303

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2671957capsaicin 0.0012 % / methyl salicylate 0.61 % Topical SolutionPSN2
2671957capsaicin 0.012 MG/ML / methyl salicylate 6.1 MG/ML Topical SolutionSCD2
2671957capsaicin 0.0012 % / methyl salicylate 0.61 % Topical SolutionSY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CAPSICUM Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52000-303-34Universal ARTHRITIS and SPORT473 mL in 1 BOTTLE, PLASTICLIQUID4732

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52000-303UNIVERSAL ARTHRITIS AND SPORT (METHYL SALICYLATE, CAPSICUM) LIQUID [UNIVERSAL DISTRIBUTION CENTER LLC]2Current NDC, 1 package rows20241212_7f067e95-e01c-4b9a-a02e-0af097beb18c.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52000-30352000-303-34

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
Universal ARTHRITIS and SPORTMETHYL SALICYLATE, CAPSICUMUniversal Distribution Center LLC7f067e95-e01c-4b9a-a02e-0af097beb18c2024-11-22WarningsExact identifier
ndc (package): 52000-303-34
ndc (product): 52000-303
ndc11 (package): 52000030334
spl id: a3f759bb-a70e-44d5-83e1-5311fe9bb048
spl set id: 7f067e95-e01c-4b9a-a02e-0af097beb18c

Reported adverse events (FAERS/openFDA)#

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