Pain Relief

Manufacturer
Derma Care Research Labs, LLC
Effective date
2019-06-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:20:08

Label at a glance#

ProductPain Relief CopperGel
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Camphor 3.5%, Menthol 3.5%

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.

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, or if redness or irritation develops.

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

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Blue 1, Copper PCA, Ethyhexylglycerin, Eucalyptus Globulus Leaf Oil, Glycerin, Isopropyl Alcohol, Phenoxyethanol, Water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

cartoncarton

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72839-25372839-253-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
b8e350c4-bc83-6daf-e053-2a95a90a794f8c5259bd-7fe0-f239-e053-2995a90a0a0f2021-01-14WarningsExact identifier
spl set id: 8c5259bd-7fe0-f239-e053-2995a90a0a0f

Reported adverse events (FAERS/openFDA)#

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