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
2026-09-28
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/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:44:17
Harmonized routes table
Harmonized routes
TOPICAL

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.