PUREGEN LABS Pain Relief 4 Lidocaine

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
PUREGEN LABS Pain Relief 4 Lidocaine
Generic name
LIDOCAINE
Manufacturer
Advanced Rx LLC
Product type
HUMAN OTC DRUG
SPL set ID
9dff40d8-8d7e-4629-bea5-987f5e68477d
SPL ID
1a99684d-b57c-8eac-e063-6294a90aae2e
Version
1
Effective date
2024-06-11
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:24:24
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 more than 1 patch at a time on wounds or damaged skin with a heating pad If you are allergic to any ingredients of this product When using this product Avoid contact with the eyes Stop use and ask a doctor if localized skin reactions occur, such as rash, itching, redness, irritation condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use

Reported adverse events (FAERS/openFDA)#

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