CopperFixx

Manufacturer
Quest Products, Inc. | Filltech USA, LLC
Effective date
2024-11-05
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 02:28:49

Label at a glance#

ProductCopperFixx
Active ingredientCOPPER, ARNICA MONTANA
Label structure7 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with: arthritis, simple backache, strains, and bruises.

Dosage and administration

Adults and children over 12 years: Ask a doctor before use in children under 12 years of age . Apply liberally to affected area. Massage gently until completely absorbed. Repeat as needed WASH HANDS WITH SOAP AND WATER AFTER APPLYING

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active IngredientsPurpose
"HPUS" indicates the active ingredients are in the official Homeopathic Pharmacopoeia of the United States.
Cuprum Metallicum 11X HPUSMuscle cramps, spasms
Arnica Montana 4X HPUSSprains, Pain

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with: arthritis, simple backache, strains, and bruises.

Warnings

WARNINGS SECTION

OTC - DO NOT USE SECTION

Do not use if seal is broken or missing.

SPL UNCLASSIFIED SECTION

If symptoms persist for more than 7 days or worsen, contact a licensed health care provider.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN. For external use only. If swallowed, contact a Poison Control Center. Do not use on open wounds. Avoid contact with eyes or other mucus membranes. If contact occurs, rinse thoroughly with water.

Stop use and consult a doctor if

OTC - STOP USE SECTION

Condition worsens- symptoms persist for more than 7 days or clear up and occur again within a few days- redness is present- irritation develops. If pregnant or breast- feeding, ask a health professional before use.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children over 12 years:

  • Ask a doctor before use in children under 12 years of age.
  • Apply liberally to affected area.
  • Massage gently until completely absorbed.
  • Repeat as needed
  • WASH HANDS WITH SOAP AND WATER AFTER APPLYING

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Water, Isopropyl Myristate, Cetearyl Alcohol, Behentrimonium Methosulfate, Polysorbate 60, Cetyl Alcohol, Cocos Nucifera (Coconut) Oil, Persea Gratissima (Avocado) Oil, Simmondsia Chinensis (Jojoba) Seed Oil, Stearic Acid, , Butylene Glycol, Dimethicone, Vanillyl Butyl Ether, Hydrolyzed Silk, Silk Amino Acids, Sodium Lactate, Tocopherol, Allantoin, Lavandula Angustifolia (Lavender) Oil, Disodium EDTA, Diazolidinyl Urea, Sodium Benzoate, Potassium Sorbate, Citrus Medica Limonum (Lemon) Peel Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil.

PRINCIPAL DISPLAY PANEL - 57 g Jar Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

COPPER FIXX®

PAIN RELIEF CREAM

Powered by Copper

Heat Technology with Arnica

  • Muscle Pain and Stiffness
  • Joint Inflammation
  • Increases Blood Flow

Net Wt. 2 FL OZ/57g

pdppdp

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c599c4a0-705d-4ebb-ab1f-977af038f96aProduct name120251124
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68229-502-022021-08-20C16284748780-19d75b9cf-e990-f424-e053-dadaa90a57ceCopperFixx™
68229-502-022020-01-31C16284748780-19d75b9cf-e990-f424-e053-dadaa90a57ceCopperFixx™

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68229-502-01CopperFixx57 g in 1 JAROINTMENT577
68229-502-02CopperFixx1 in 1 CARTONOINTMENT17

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68229-502COPPERFIXX (COPPER AND ARNICA MONTANA) OINTMENT [QUEST PRODUCTS, INC.]7Current NDC, Legacy NDC, 2 package rows20241107_ff2d3197-a8f3-46ff-899d-670a953d41d5.zip

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68229-50268229-502-01, 68229-502-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 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
CopperFixxCOPPER AND ARNICA MONTANAQuest Products, Inc.ff2d3197-a8f3-46ff-899d-670a953d41d52024-11-05WarningsExact identifier
ndc (package): 68229-502-02
ndc (package): 68229-502-01
ndc (product): 68229-502
ndc11 (package): 68229050201
ndc11 (package): 68229050202
spl id: 262e370a-db08-cf2d-e063-6394a90ab0bc
spl set id: ff2d3197-a8f3-46ff-899d-670a953d41d5

Reported adverse events (FAERS/openFDA)#

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