FDA.reportPublic FDA data

Arthritis Relief Cream

Manufacturer
NewMarket Health Products LLC | Mariposa Labs LLC
Effective date
2017-10-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:37

Label at a glance#

ProductArthritis Relief
Active ingredientMENTHOL
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Menthol 1.25%

OTC - PURPOSE SECTION

Purpose

Topical Analgesic

INDICATIONS & USAGE SECTION

Use   Temporarily relieves minor aches and pains of muscles and joints associated with:

  • simple backache
  • arthritis
  • strains
  • bruises
  • sprains

DOSAGE & ADMINISTRATION SECTION

Directions

  • Adult 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.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: aloe vera gel, cetyl alcohol, cetyl esters (proprietary blend of esterfied fatty acids), cinnamon oil, eucalyptus oil, glyceryl stearate, grape seed oil, hypromellose, jojoba oil, peppermint oil, phenoxyethanol, potassium sorbate, purified water, sodium benzoate, squalane, stearic acid, stearyl alcohol, tea tree oil, vegetable glycerin, wintergreen oil.

OTC - QUESTIONS SECTION

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

Refill Code: K650T4AA

Manufactured for and Distributed by NewMarket Health

Products, LLC. 1125 N. Charles St., Baltimore, MD 21201

Made in the USA from foreign and domestic ingredients.

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use

  • on wounds or damaged skin

OTC - WHEN USING SECTION

When using this product

  • avoid contact with eyes or mucous membranes
  • do not bandage tightly

OTC - STOP USE SECTION

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

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

North Star 

Nutritionals 

PARABEN FREE!

Arthritis Relief Cream 

Pain Relieving Cream

with Menthol 

Net Wt. 2 oz (57ml)

Arthritis Relief Cream LabelArthritis Relief Cream Label

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
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50972-274-012020-01-31C16284748780-19d75b9cf-dd12-f424-e053-dadaa90a57ceArthritis Relief Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50972-274-01Arthritis Relief57 mL in 1 TUBECREAM571

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50972-274ARTHRITIS RELIEF (MENTHOL) CREAM [NEWMARKET HEALTH PRODUCTS LLC]1Legacy NDC, 1 package rows20171004_150c99f8-4a5b-43f6-b13c-788c6f4e69bc.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50972-27450972-274-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
ALOE VERA LEAFZY81Z83H0XIACT
CETYL ALCOHOL936JST6JCNIACT
CETYL ESTERS WAXD072FFP9GUIACT
CINNAMON OILE5GY4I6YCZIACT
EUCALYPTUS OIL2R04ONI662IACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
GRAPE SEED OIL930MLC8XGGIACT
HYPROMELLOSES3NXW29V3WOIACT
JOJOBA OIL724GKU717MIACT
PEPPERMINT OILAV092KU4JHIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT
SQUALANEGW89575KF9IACT
STEARIC ACID4ELV7Z65APIACT
STEARYL ALCOHOL2KR89I4H1YIACT
TEA TREE OILVIF565UC2GIACT
GLYCERINPDC6A3C0OXIACT
METHYL SALICYLATELAV5U5022YIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM BENZOATEOJ245FE5EUIACT

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
761de70d-59dc-48f1-a248-f689de9a33c0150c99f8-4a5b-43f6-b13c-788c6f4e69bc2017-10-04WarningsExact identifier
spl id: 761de70d-59dc-48f1-a248-f689de9a33c0
spl set id: 150c99f8-4a5b-43f6-b13c-788c6f4e69bc

Reported adverse events (FAERS/openFDA)#

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