OTC - ACTIVE INGREDIENT SECTION
Camphor 3.5%, Menthol 3.5%
CBD Pain Relief
- Manufacturer
- Derma Care Research Labs, LLC
- Effective date
- 2019-06-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:20:08
Label at a glance#
ProductCBD Pain Relief CopperGel
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure8 sections
Label contents#
Full prescribing information#
OTC - PURPOSE SECTION
Topical Analgesic
DOSAGE & ADMINISTRATION SECTION
For the temporary relief of itching associated with minor aches and pains in muscles and joints associated with strains, sprains, arthritis, and bruises.
WARNINGS SECTION
For external use only.
Flammable--Do not use while smoking or near heat or flame.
When using this product keep out of eyes, do not apply to wounds or damaged skin, do not bandage tightly, contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F.
Stop use and ask a doctor if condition worsens or symptoms persist for more than 7 days if symptoms clear up and occur again within a few days.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
INDICATIONS & USAGE SECTION
Clean the affected area before applying products. 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: ask a doctor.
INACTIVE INGREDIENT SECTION
Alcohol Denat., Aloe Barbadensis Leaf Extract, Arnica Montana Extract, BHT, CBD Hemp Extract, Chamomilla Recutita (Matricaria) Flower Extract, Copper PCA, Dimethyl Sulfone, Eucalyptus Globulus Leaf Oil, Mentha Piperita (Peppermint) Oil, Propylene Glycol, Water.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- CBD Pain Relief CopperGel
- Camphor 3.5%, Menthol 3.5%
- ALCOHOL
- ALOE VERA LEAF
- ARNICA MONTANA
- CAMPHOR (SYNTHETIC)
- BUTYLATED HYDROXYTOLUENE
- CANNABIDIOL
- CHAMAEMELUM NOBILE FLOWER
- COPPER PIDOLATE
- DIMETHYL SULFONE
- EUCALYPTUS OIL
- PEPPERMINT OIL
- PEPPERMINT
- PROPYLENE GLYCOL
- WATER
- MENTHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72839-199 | 72839-199-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| ARNICA MONTANA | O80TY208ZW | IACT |
| CAMPHOR (SYNTHETIC) | 5TJD82A1ET | ACTIB |
| BUTYLATED HYDROXYTOLUENE | 1P9D0Z171K | IACT |
| CANNABIDIOL | 19GBJ60SN5 | IACT |
| CHAMAEMELUM NOBILE FLOWER | O2T154T6OG | IACT |
| COPPER PIDOLATE | 497G7G1SL1 | IACT |
| DIMETHYL SULFONE | 9H4PO4Z4FT | IACT |
| EUCALYPTUS OIL | 2R04ONI662 | IACT |
| PEPPERMINT OIL | AV092KU4JH | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| WATER | 059QF0KO0R | IACT |
| MENTHOL | L7T10EIP3A | ACTIB |
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 |
|---|---|---|---|---|---|---|
| b984ddf4-b057-979c-e053-2995a90a1b60 | 8c4fd148-ca77-66ee-e053-2a95a90af06e | 2021-01-22 | Warnings | 8c4fd148-ca77-66ee-e053-2a95a90af06e |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.