OrthoNesic Pain Relieving Gel

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
OrthoNesic Pain Relieving Gel
Generic name
MENTHOL, CAMPHOR
Manufacturer
Blaine Labs Inc.
Product type
HUMAN OTC DRUG
SPL set ID
122f60c2-f8df-4625-8bb8-a2244a261b5d
SPL ID
a8fe10de-60fb-4197-a42c-37802f676b53
Version
1
Effective date
2026-07-01
Source export date
2026-11-06
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:04:03
Harmonized routes table
Harmonized routes
CUTANEOUS

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 extrenal use only Do not use: ■ on wounds or damaged skin ■ with a heating pad When using this product : ■ avoid contact with eyes or mucous membranes ■ do not bandage tightly Stop use and ask a physician if : ■ condition worsens ■ symptoms persist for more than 7 days or clear up and occur again within a few days ■ excessive skin irritation develops.

Reported adverse events (FAERS/openFDA)#

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