Dosage and administration
Adults over 21 years: Apply a small amount to the affected area. Massage in circular motion until absorbed. Repeat as needed, but no more than 3 to 4 times per day. Wash hands with soap and water after use.
Adults over 21 years: Apply a small amount to the affected area. Massage in circular motion until absorbed. Repeat as needed, but no more than 3 to 4 times per day. Wash hands with soap and water after use.
Camphor 2%
Menthol 6%
Topical Analgesic
Aid for temporary local relief of minor pain in muscles or joints.
For external use only.
Ask a doctore before use if you have redness over affected area
Use only as directed.
Do not bandage tightly
Do not use with heating pad, pack, wrap hot water bottle or any heating element.
Avoid contact with eyes.
Do not apply to wounds or damaged, broken, or irritated skin.
Do not expose the area treated with product to heat or direct sunlight.
Condition worsens.
Redness is present.
Irritation develops.
Symptoms persist for more than 7 days or clear up occur again within a few days.
You experience signs injury, such as pain, swelling or blistering where the product was applied.
Ask a health professional before use.
If swallowed, get medical help or contact a Poison Control Center right away.
Adults over 21 years:
Apply a small amount to the affected area.
Massage in circular motion until absorbed.
Repeat as needed, but no more than 3 to 4 times per day.
Wash hands with soap and water after use.
Store tightly closed in a dry place at controlled temperature between 59°-86° F (15°-30° C).
This product is intended only for use by healthy adults aged 21 years & older.
Water (Aqua), Propylene Glycol, Alcohol Denat, Polysorbate 20, Mentha Piperita (Peppermint) Oil, Cannabidiol, Rosmarinus Officinalis (Rosemary) Oil, Thymus Vulgaris (Thyme) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Carbomer, Sodium Hydroxide, Benzyl Alcohol, Salicylic Acid, Glycerin, Sorbic Acid, FD&C Blue. 1 Powder (CI 42090), FD&C Yellow. 5 (CI 19140), Limonene.
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0696831876794 | GTIN-13: 0696831876794 EAN-13: 0696831876794 GTIN-12: 696831876794 UPC-A: 696831876794 GTIN storage (14 digits): 00696831876794 | FD-04267 JUST CBD - ULTRA RELIEF GEL 1000 CBD VER 2 73647-602-04.jpg |
| QR code link | QR Code | FD-04268 JUST CBD - ULTRA RELIEF GEL 5000 CBD VER 2 73647-206-04.jpg, FD-04267 JUST CBD - ULTRA RELIEF GEL 1000 CBD VER 2 73647-602-04.jpg |
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 4d7a96d5-8256-4268-9a6c-25ea66d321fe | Product name | 1 | 20180814 |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73647-206-04 | JUST CBD ULTRA RELIEF | 118 mL in 1 BOTTLE, PUMP | GEL | 118 | 3 | |
| 73647-602-04 | JUST CBD ULTRA RELIEF | 118 mL in 1 BOTTLE, PUMP | GEL | 118 | 3 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 73647-206 | 73647-206-04 |
| 73647-602 | 73647-602-04 |
Every source-derived ingredient row is available through these pages.
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 |
|---|---|---|---|---|---|---|
| 43d6b434-3f26-f948-e063-6294a90ad22e | f65327b3-9c97-58f3-e053-2995a90a3f55 | 2025-11-17 | Warnings | 43d6b434-3f26-f948-e063-6294a90ad22e f65327b3-9c97-58f3-e053-2995a90a3f55 |
Adverse event summaries are temporarily unavailable. Other product information remains available.