3% Menthol plus 0.083% Capsaicin Pain Relief Patch

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: 3% Menthol plus 0.083% Capsaicin Pain Relief Patch
Generic name: PAIN RELIEF PATCH, PAIN RELIEF STRIP
Manufacturer: Xuzhou Lanting Pharmaceutical Co., Ltd
Product type: HUMAN OTC DRUG
SPL set ID: 378a6887-c609-b79c-e063-6394a90a00f4
SPL ID: 3d3c3329-1851-acbc-e063-6294a90abecb
Version: 3
Effective date: 2025-06-10
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 05:20:04

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		3% Menthol plus 0.083% Capsaicin Pain Relief Patch	openfda.brand_name
generic name		PAIN RELIEF PATCH, PAIN RELIEF STRIP	openfda.generic_name
manufacturer name		Xuzhou Lanting Pharmaceutical Co., Ltd	openfda.manufacturer_name
ndc	package	85323-008-01	openfda.package_ndc
ndc	product	85323-008	openfda.product_ndc
ndc11	package	85323000801	derived:openfda.package_ndc
rxcui		2287163	openfda.rxcui
spl id		3d3c3329-1851-acbc-e063-6294a90abecb	id
spl set id		378a6887-c609-b79c-e063-6394a90a00f4	set_id
unii		S07O44R1ZM	openfda.unii
unii		L7T10EIP3A	openfda.unii

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 WARNINGS: EXTERNAL USE ONLY When using this product use only as directed do not bandage tightly or use with a heating pad aviod contact with eyes and mucous membranes do not apply to wounds or damaged skin Stop use and ask a doctor condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days redness is present skin irritation develops If pregnant or breast-feeding, ask a health professional before use. KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Reported adverse events (FAERS/openFDA)#

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