CopperFixx

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: CopperFixx
Generic name: COPPER AND ARNICA MONTANA
Manufacturer: Quest Products, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: ff2d3197-a8f3-46ff-899d-670a953d41d5
SPL ID: 262e370a-db08-cf2d-e063-6394a90ab0bc
Version: 7
Effective date: 2024-11-05
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:27:56

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		CopperFixx	openfda.brand_name
generic name		COPPER AND ARNICA MONTANA	openfda.generic_name
manufacturer name		Quest Products, Inc.	openfda.manufacturer_name
ndc	package	68229-502-02	openfda.package_ndc
ndc	package	68229-502-01	openfda.package_ndc
ndc	product	68229-502	openfda.product_ndc
ndc11	package	68229050201	derived:openfda.package_ndc
ndc11	package	68229050202	derived:openfda.package_ndc
spl id		262e370a-db08-cf2d-e063-6394a90ab0bc	id
spl set id		ff2d3197-a8f3-46ff-899d-670a953d41d5	set_id
unii		789U1901C5	openfda.unii
unii		O80TY208ZW	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Do not use if seal is broken or missing. If symptoms persist for more than 7 days or worsen, contact a licensed health care provider. 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 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.

Reported adverse events (FAERS/openFDA)#

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