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#
Contacts and useful links#
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
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)
DailyMed RxNorm Mappings#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Data code | Code 128 | B071Z3472D | 001 label.jpg |
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6c13b22c-b3ba-4127-b768-0132dd5ab0d1 | Product name | 1 | 20230829 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 87282-001-01 | Joint and Muscle Relief | 89 mL in 1 JAR | CREAM | 89 | 1 | |
| 87282-001-02 | Joint and Muscle Relief | 100 mL in 1 BOTTLE, PUMP | CREAM | 100 | 1 |
Products#
Every source-derived product name is available through these pages.
- Joint and Muscle Relief
- menthol
- CARBOMER
- POLYSORBATE 20
- ALPHA-TOCOPHEROL ACETATE
- ILEX PARAGUARIENSIS LEAF
- DIMETHYL SULFONE
- EDETATE DISODIUM
- GLYCERIN
- ISOPROPYL ALCOHOL
- WATER
- CAPRYLYL GLYCOL
- MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL
- ALOE BARBADENSIS LEAF JUICE
- GLYCERYL LAURATE
- PYRIDOXINE HCL
- TRIETHANOLAMINE
- ARNICA MONTANA
- GLYCERYL 1-UNDECYLENATE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 87282-001 | 87282-001-01, 87282-001-02 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Joint and Muscle Relief | MENTHOL | Smart Cookie Solutions Inc. | 45c24d56-4dc9-2884-e063-6294a90a52cc | 2025-12-12 | Warnings | 87282-001-02 87282-001-01 87282-001 87282000101 87282000102 45c24d56-4dca-2884-e063-6294a90a52cc 45c24d56-4dc9-2884-e063-6294a90a52cc |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
