Profoot Pain Relief Patches

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: Profoot Pain Relief Patches
Generic name: CAMPHOR, MENTHOL, METHYL SALICYLATE
Manufacturer: Rooftop Consumer Health, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: cc011b79-2761-40f7-8142-88f8e30a179a
SPL ID: 252a039c-519e-39ba-e063-6394a90ab32c
Version: 19
Effective date: 2024-10-23
Source export date: 2026-09-28
Source partition: 11
Source file: https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:15:36

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Profoot Pain Relief Patches	openfda.brand_name
generic name		CAMPHOR, MENTHOL, METHYL SALICYLATE	openfda.generic_name
manufacturer name		Rooftop Consumer Health, Inc.	openfda.manufacturer_name
ndc	package	29784-121-36	openfda.package_ndc
ndc	package	29784-122-36	openfda.package_ndc
ndc	package	29784-600-01	openfda.package_ndc
ndc	product	29784-600	openfda.product_ndc
ndc11	package	29784060001	derived:openfda.package_ndc
ndc11	package	29784012236	derived:openfda.package_ndc
ndc11	package	29784012136	derived:openfda.package_ndc
rxcui		853260	openfda.rxcui
spl id		252a039c-519e-39ba-e063-6394a90ab32c	id
spl set id		cc011b79-2761-40f7-8142-88f8e30a179a	set_id

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 For external use only If prone to allergic reaction from aspirin or salicylates, consult a doctor before use. Allergy alert: Do not use • on wounds or damaged skin • with a heating pad • if you are allergic to any of the ingredients of this product When using this product • use only as directed • avoid contact with the eyes, mucous membranes or rashes • do not bandage tightly Stop use and ask a doctor if • rash, itching or excessive skin irritation develops • condition worsens •symptoms persist for more than 7 days • symptoms clear up and occur again within a few days ask a health professional before use. If pregnant or breastfeeding,

Reported adverse events (FAERS/openFDA)#

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