Professional Therapy MuscleCare pain relieving gel Extra Strength

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 gel Extra Strength
Generic name: CAMPHOR, MENTHOL
Manufacturer: Active and Innovative Inc.
Product type: HUMAN OTC DRUG
SPL set ID: 1d2403d9-99c3-24f5-e054-00144ff8d46c
SPL ID: 39bd979f-91a1-0554-e054-00144ff8d46c
Version: 2
Effective date: 2016-08-10
Source export date: 2026-10-27
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:56:21

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		part348	openfda.application_number
brand name		Professional Therapy MuscleCare pain relieving gel Extra Strength	openfda.brand_name
generic name		CAMPHOR, MENTHOL	openfda.generic_name
manufacturer name		Active and Innovative Inc.	openfda.manufacturer_name
ndc	package	70039-283-07	openfda.package_ndc
ndc	product	70039-283	openfda.product_ndc
ndc11	package	70039028307	derived:openfda.package_ndc
rxcui		1039731	openfda.rxcui
spl id		39bd979f-91a1-0554-e054-00144ff8d46c	id
spl set id		1d2403d9-99c3-24f5-e054-00144ff8d46c	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.