GoodSense Cooling Pain Relief

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
GoodSense Cooling Pain Relief
Generic name
MENTHOL
Manufacturer
Geiss, Destin & Dunn, Inc
Product type
HUMAN OTC DRUG
SPL set ID
2e5e1375-df07-9a43-e063-6394a90a9938
SPL ID
3a5d55cc-6cda-ca90-e063-6294a90a6843
Version
2
Effective date
2025-07-20
Source export date
2026-09-28
Source partition
3
Source file
https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:20:37
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

For external use only . When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water, avoid contact with broken skin, do not bandage tightly, and do not use with heating pad. Stop use and ask a doctor if the condition worsens, rash or irritation develops and lasts for more than 7 days or clear up and occur again within a few days.

Reported adverse events (FAERS/openFDA)#

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