Copperlife Foot

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: Copperlife Foot
Generic name: DIMETHICONE 1%
Manufacturer: Tommie Copper, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: cb825d2c-6333-3c1f-e053-2995a90a78f3
SPL ID: 29591578-c165-5ed4-e063-6394a90a7df3
Version: 3
Effective date: 2024-12-15
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:20:47

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Copperlife Foot	openfda.brand_name
generic name		DIMETHICONE 1%	openfda.generic_name
manufacturer name		Tommie Copper, Inc.	openfda.manufacturer_name
ndc	package	72562-211-01	openfda.package_ndc
ndc	product	72562-211	openfda.product_ndc
ndc11	package	72562021101	derived:openfda.package_ndc
spl id		29591578-c165-5ed4-e063-6394a90a7df3	id
spl set id		cb825d2c-6333-3c1f-e053-2995a90a78f3	set_id
unii		92RU3N3Y1O	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

For external use only. When using this product do not get into eyes. Stop use and ask a doctor if condition worsens, if symptoms persist for more than 7 days or clear up and occur again within a few days. Do not use on deep puncture wounds, animal bites, and serious burns.

Reported adverse events (FAERS/openFDA)#

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