Pain Relief Muscle

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: Pain Relief Muscle
Generic name: CAMPHOR (NATURAL)
Manufacturer: J.R. Watkins, LLC.
Product type: HUMAN OTC DRUG
SPL set ID: 1dc21c95-b419-4175-85f8-040b73060d37
SPL ID: 141bf837-5a0f-da26-e063-6294a90a20bc
Version: 2
Effective date: 2024-03-20
Source export date: 2026-10-27
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/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:12:40

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Pain Relief Muscle	openfda.brand_name
generic name		CAMPHOR (NATURAL)	openfda.generic_name
manufacturer name		J.R. Watkins, LLC.	openfda.manufacturer_name
ndc	package	72342-200-16	openfda.package_ndc
ndc	product	72342-200	openfda.product_ndc
ndc11	package	72342020016	derived:openfda.package_ndc
rxcui		2469136	openfda.rxcui
spl id		141bf837-5a0f-da26-e063-6294a90a20bc	id
spl set id		1dc21c95-b419-4175-85f8-040b73060d37	set_id
unii		N20HL7Q941	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. Do Not Use On open wounds, damaged or irriated skin With a heating pad or TENS device With any other creams, ointments, sprays, liniments, or other topical products containing camphor When using this product Do not bandage tightly Use only as directed Avoid contact with eyes or mucous membranes Stop use and ask a doctor if Condition worsens Rash, itching, redness, or excessive irritation of skin develops Symptoms persist for more than 7 days Symptoms clear up and occur again within a few days If pregnant or breastfeeding Ask a health professional before use. Keep out of reach of children If swallowed, get medical help or contact Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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