POMG NIGHT TIME 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 NIGHT TIME PAIN RELIEF ROLLER
Generic name
LIDOCAINE HYDROCHLORIDE
Manufacturer
POMG LLC
Product type
HUMAN OTC DRUG
SPL set ID
28d7dfb0-a94c-90de-e063-6294a90a036a
SPL ID
44fe3ce1-757c-b6ea-e063-6294a90a012c
Version
3
Effective date
2025-12-02
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 05:46:34
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.