Arthritis Relief Cream

Manufacturer
NewMarket Health Products LLC
Effective date
2021-01-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:07

Label at a glance#

ProductArthritis Relief Cream
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: Apply to affected area not more than 3 to 4 times daily. • Children under 12 years of age: Consult a physician.

Label contents#

Full prescribing information#

Active Ingredient section

OTC - ACTIVE INGREDIENT SECTION

 Menthol, Unspecified Form   1.25%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

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.

Do not use

• On wounds or damaged skin

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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: Consult a physician.

Other Information.

SPL UNCLASSIFIED SECTION

Questions? Need to refill? 1-800-895-2108

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Vera Gel, Cetyl Alcohol, Cetyl Esters (proprietary blend of esterified fatty acids), Cinnamon Oil, Eucalyptus Oil, Glyceryl Stearate, Grape Seed Oil, Hypromellose, Jojoba Oil, Olive Oil, Peppermint Oil, Phenoxyethanol, Potassium Sorbate, Purified Water, Sodium Benzoate, Squalane, Stearic Acid, Stearyl Alcohol, Tea Tree Oil, Vegetable Glycerin, Wintergreen Oil.

Product Image

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
416982menthol 1.25 % Topical CreamPSN1
416982menthol 12.5 MG/ML Topical CreamSCD1
416982menthol 1.25 % Topical CreamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50972-275-012023-01-30C16284748780-1f386c64a-283f-0266-e053-dadaa90a7c1aArthritis Relief Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50972-275-01Arthritis Relief Cream57 mL in 1 TUBECREAM571

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50972-275ARTHRITIS RELIEF CREAM (MENTHOL) CREAM [NEWMARKET HEALTH PRODUCTS LLC]1Legacy NDC, 1 package rows20210121_6004a5f1-4f83-47da-8b1e-6d62e41c4c2e.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50972-27550972-275-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
b9556394-7d28-64aa-e053-2a95a90ad8ff6004a5f1-4f83-47da-8b1e-6d62e41c4c2e2021-01-20WarningsExact identifier
spl id: b9556394-7d28-64aa-e053-2a95a90ad8ff
spl set id: 6004a5f1-4f83-47da-8b1e-6d62e41c4c2e

Reported adverse events (FAERS/openFDA)#

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