Professional Therapy MuscleCare Pro

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
Generic name: MENTHOL AND CAMPHOR
Manufacturer: ACTIVE AND INNOVATIVE, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 17961a84-6bee-c75f-e063-6394a90af576
SPL ID: 17961a30-5dd4-cae6-e063-6394a90a3faf
Version: 3
Effective date: 2024-05-03
Source export date: 2026-10-12
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:53:56

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Professional Therapy MuscleCare Pro	openfda.brand_name
generic name		MENTHOL AND CAMPHOR	openfda.generic_name
manufacturer name		ACTIVE AND INNOVATIVE, LLC	openfda.manufacturer_name
ndc	package	70039-303-04	openfda.package_ndc
ndc	package	70039-303-32	openfda.package_ndc
ndc	package	70039-303-16	openfda.package_ndc
ndc	product	70039-303	openfda.product_ndc
ndc11	package	70039030316	derived:openfda.package_ndc
ndc11	package	70039030332	derived:openfda.package_ndc
ndc11	package	70039030304	derived:openfda.package_ndc
spl id		17961a30-5dd4-cae6-e063-6394a90a3faf	id
spl set id		17961a84-6bee-c75f-e063-6394a90af576	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. Caution: 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 tightly.

Reported adverse events (FAERS/openFDA)#

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