Joint & Muscle Pain Cream

Manufacturer
Shaklee Corporation
Effective date
2024-01-30
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:08:03

Label at a glance#

ProductJoint and Muscle Pain
Active ingredientMENTHOL
Label structure6 sections

Indications and uses

Provides penetrating temporary relief for minor pain in muscles and joints associated with: Backache Arthritis Bruises Sprains

Dosage and administration

Apply generously to affected area. Massage well into painful area. Repeat as necessary, but not more than 3 to 4 times daily. Adults and children over the age of 2: Do not use; consult a physician. Children under the age of 2:

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol (5%)

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

Provides penetrating temporary relief for minor pain in muscles and joints associated with:

  • Backache
  • Arthritis
  • Bruises
  • Sprains

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

  • with a heating pad. Do not apply to wounds or damaged skin. Do not bandage tightly after use.
  • Avoid contact with eyes.
  • Discontinue use and consult a physician if condition worsens, or if symptoms persist more than 7 days or 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

Apply generously to affected area. Massage well into painful area. Repeat as necessary, but not more than 3 to 4 times daily. Adults and children over the age of 2:

Do not use; consult a physician. Children under the age of 2:

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propanediol, Isononyl Isononanoate, Cetearyl Alcohol, Ethylhexyl Palmitate, Prunus Amygdalus Dulcis (Sweet Almond) Oil 1%, Phenoxyethanol, Stearic Acid, Arginine, Cetearyl Glucoside, Carbomer, Polysorbate 60, Caprylyl Glycol, Xanthan Gum, Tocopherol, Ethylhexylglycerin, Aloe Barbadensis Leaf Juice, Glycerin, Zingiber Officinale (Ginger) Root Extract.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039690menthol 5 % Topical CreamPSN5
1039690menthol 50 MG/ML Topical CreamSCD5
1039690menthol 5 % Topical CreamSY5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59899-022-00Joint and Muscle Pain85 g in 1 TUBECREAM855

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59899-022JOINT AND MUSCLE PAIN (MENTHOL) CREAM [SHAKLEE CORPORATION]5Current NDC, Legacy NDC, 1 package rows20240131_3943824f-1f4f-4d6f-bd73-0b1be02162a5.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59899-02259899-022-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 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
Joint and Muscle PainMENTHOLShaklee Corporation3943824f-1f4f-4d6f-bd73-0b1be02162a52024-01-30WarningsExact identifier
ndc (package): 59899-022-00
ndc (product): 59899-022
ndc11 (package): 59899002200
spl id: 102a5003-e856-7404-e063-6394a90a2447
spl set id: 3943824f-1f4f-4d6f-bd73-0b1be02162a5

Reported adverse events (FAERS/openFDA)#

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