Professional Therapy MuscleCare Pain Relieving

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 Pain Relieving
Generic name: MENTHOL, CAMPHOR
Manufacturer: Active and Innovative Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 42f1abeb-f6d7-01c3-e054-00144ff88e88
SPL ID: 2c670151-ca6c-8d49-e063-6394a90af091
Version: 3
Effective date: 2025-01-23
Source export date: 2026-10-30
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/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:36:44

Harmonized routes table
Harmonized routes
CUTANEOUS, 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
application number		M017	openfda.application_number
brand name		Professional Therapy MuscleCare Pain Relieving	openfda.brand_name
generic name		MENTHOL, CAMPHOR	openfda.generic_name
manufacturer name		Active and Innovative Inc.	openfda.manufacturer_name
ndc	package	70039-300-02	openfda.package_ndc
ndc	product	70039-300	openfda.product_ndc
ndc11	package	70039030002	derived:openfda.package_ndc
rxcui		900390	openfda.rxcui
spl id		2c670151-ca6c-8d49-e063-6394a90af091	id
spl set id		42f1abeb-f6d7-01c3-e054-00144ff88e88	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. 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 tightly.

Reported adverse events (FAERS/openFDA)#

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