Joint & Muscle Relief Cream

Manufacturer
Smart Cookie Solutions Inc.
Effective date
2025-12-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:25:53

Label at a glance#

ProductJoint and Muscle Relief
Active ingredientMENTHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient:

Menthol 3.70%

OTC - PURPOSE SECTION

Purpose

Topical Analgesic

INDICATIONS & USAGE SECTION

Uses

For the temporary relief of minor aches and pains of muscles and joints.

WARNINGS SECTION

Warnings: For external use only

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

When using this product • Avoid contact with the eyes. • Do not bandage tightly.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash or irritation develops and lasts, condition worsens, or if symptoms persist for more than 7 days or 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 contacct a Poison Control Center right away.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Adults and children 2 years of age and older:
  • Apply to affected area not more than 3 to 4 times daily.
  • Children under 2 years of age: consult a doctor.

Other information

SPL UNCLASSIFIED SECTION

Protect the product in this container from excessive heat and direct sun.

INACTIVE INGREDIENT SECTION

Inactive ingredients: aloe barbadensis leaf juice, arnica montana extract, caprylyl glycol, carbomer, dimethyl sulfone, disodium EDTA, glycerin, glyceryl laurate, glyceryl undecylenate, ilex paraguariensis leaf extract, isopropyl alcohol, melaleuca alternifolia (tea tree) leaf oil, polysorbate 20, pyridoxine HCl, tocopheryl acetate, triethanolamine, water(aqua).

OTC - QUESTIONS SECTION

Questions?

904-439-7618

SPL UNCLASSIFIED SECTION

Made in USA

Dist. by: Smart Cookie Solutions Inc. 10685-B Hazelhurst Dr. #18381, Houston, TX 77043

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Joint & Muscle Relief

Cream

Topical Analgesic Cream

• Arnica Extract • Ilex Extract

• Aqua • Tea Tree

• Aloe Leaf Juice

3 fl oz (89ml)

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1655936menthol 3.7 % Topical CreamPSN1
1655936menthol 37 MG/ML Topical CreamSCD1
1655936menthol 3.7 % Topical CreamSY1

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128B071Z3472D001 label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87282-001-01Joint and Muscle Relief89 mL in 1 JARCREAM891
87282-001-02Joint and Muscle Relief100 mL in 1 BOTTLE, PUMPCREAM1001

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87282-00187282-001-01, 87282-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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 ReliefMENTHOLSmart Cookie Solutions Inc.45c24d56-4dc9-2884-e063-6294a90a52cc2025-12-12WarningsExact identifier
ndc (package): 87282-001-02
ndc (package): 87282-001-01
ndc (product): 87282-001
ndc11 (package): 87282000101
ndc11 (package): 87282000102
spl id: 45c24d56-4dca-2884-e063-6294a90a52cc
spl set id: 45c24d56-4dc9-2884-e063-6294a90a52cc

Reported adverse events (FAERS/openFDA)#

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