Green Compass Reduce Pain Relief with Menthol

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
Green Compass Reduce Pain Relief with Menthol
Generic name
MENTHOL
Manufacturer
Green Compass, Inc.
Product type
HUMAN OTC DRUG
SPL set ID
0a0c212e-ae5d-8505-e063-6394a90af622
SPL ID
2c7baad3-2add-ba3f-e063-6294a90a3bb3
Version
2
Effective date
2025-01-01
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 20:13:21
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Do not use on wounds or damaged skin with a heating pad When using this product avoid contact with the eyes do not bandage tightly Stop use and ask a doctor if condition worsens symptoms last more than 7 days condition clears up and occurs again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

Reported adverse events (FAERS/openFDA)#

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