Professional Therapy MuscleCare Pro Pain Relieving Cold Gel

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: Professional Therapy MuscleCare Pro Pain Relieving Cold Gel
Generic name: CAMPHOR, MENTHOL
Manufacturer: ACTIVE AND INNOVATIVE, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 1794c512-5f42-4ec3-e063-6394a90a87cd
SPL ID: 1794c494-425d-3eee-e063-6394a90aa08d
Version: 5
Effective date: 2024-05-03
Source export date: 2026-09-28
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/6784607726c827491ceaeab30d843632e0660ee8008c535197be5ed9e1e52201/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:03:09

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Professional Therapy MuscleCare Pro Pain Relieving Cold Gel	openfda.brand_name
generic name		CAMPHOR, MENTHOL	openfda.generic_name
manufacturer name		ACTIVE AND INNOVATIVE, LLC	openfda.manufacturer_name
ndc	package	70039-302-16	openfda.package_ndc
ndc	package	70039-302-32	openfda.package_ndc
ndc	product	70039-302	openfda.product_ndc
ndc11	package	70039030216	derived:openfda.package_ndc
ndc11	package	70039030232	derived:openfda.package_ndc
rxcui		1039731	openfda.rxcui
spl id		1794c494-425d-3eee-e063-6394a90aa08d	id
spl set id		1794c512-5f42-4ec3-e063-6394a90a87cd	set_id
unii		L7T10EIP3A	openfda.unii
unii		5TJD82A1ET	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: For external use only. Catution: Discontinue use if excessive irritation of the skin develops. Avoid getting into eyes or on mucous membranes. If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor. Do not apply to wounds or damaged skin. Do not bandage tighlty.

Reported adverse events (FAERS/openFDA)#

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