FDA.reportPublic FDA data

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
2026-08-01
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/2026-08-01/d245bd7ce31d1d8ed63276109973402ece6c44860774da30f25b731cd7418983/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:34:28
Harmonized routes table
Harmonized routes
TOPICAL

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.