POMG PAIN RELIEF ROLLER

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
POMG PAIN RELIEF ROLLER
Generic name
LIDOCAINE HYDROCHLORIDE, MENTHOL
Manufacturer
POMG LLC
Product type
HUMAN OTC DRUG
SPL set ID
1fa980fb-fc0e-fdd0-e063-6394a90adc13
SPL ID
47d03794-85ef-f653-e063-6294a90a9c17
Version
6
Effective date
2026-01-07
Source export date
2026-10-12
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:14:30
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 • If you are allergic to any ingredients in this product • On open sores and wounds • In large quantities When using this product • Use only as directed • Do not bandage tightly • Avoid contact with eyes and other mucous membranes • Do not expose the area to external heat or direct sunlight Stop use and consult a doctor if • Conditions worsen or symptoms persist for more than 7 days • Symptoms clear up and occur again within a few days • Redness is present or excessive skin irritation occurs • You experience severe burning pain, swelling, or blistering where product was applied • Allergic reaction occurs • If pregnant or breast-feeding, consult a doctor before use • Keep out of reach of children and pets. 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.