FDA.reportPublic FDA data

Lumbar Pain Relief Patch

Manufacturer
Guangzhou Hongboyuan Trading Co., Ltd. | Henan Jifutang Biotechnology Co., Ltd.
Effective date
2023-10-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:56:39

Label at a glance#

ProductLumbar Pain Relief Patch
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure11 sections

Storage and handling

Shelf Life: Two Years Other information: Sealed packaging, please keep in a cool and dark place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient: Menthol 2.5g/100g, Camphor 0.5g/100g （synthesis）

OTC - PURPOSE SECTION

Purpose: Topical analgesic

INDICATIONS & USAGE SECTION

Use to: Temporarily relieving mild pain related: arthritis, simple back pain, muscle strain, bruisinga

DOSAGE & ADMINISTRATION SECTION

Directions: Open the package and remove the backing paper, apply the cream to the shoulder or the pain, the application can be applied for 8-12 hours.

WARNINGS SECTION

Precautions:

1. This product is an external product, do not take it internally;

2. This product is a health care product and does notreplace drugs and medical devices for treatment;

3. Pregnant women, infants, breastfeeding, and those allergic to this product are prohibited;

4. Do not use skin allergies, skin damage, skin diseases and other symptoms;

5. If the skin appears red, itchy and other abnormal conditions during use, please suspend use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Same as WARNINGS SECTION

OTC - QUESTIONS SECTION

Questions or comments? +8617846992567

INACTIVE INGREDIENT SECTION

Inactive ingredients: Chinese wolfberry, myrtle, safflower, turmeric, Garden White Three Stems, Chuanxiong Root, Clematis florida, Sanqi and Root, alfalfa, camphor, etc

STATEMENT OF IDENTITY SECTION

Produced by:
Henan Jifutang Biotechnology Co..Ltd.

No.666, South 600 Miludong, Xiaomaying Village, Pushan Town,Wolong District, Nanyang City.
OEM Company:Guangzhou Hongboyuan Trading Co.,Ltd.

STORAGE AND HANDLING SECTION

Shelf Life: Two Years

Other information: Sealed packaging, please keep in a cool and dark place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

see label Lumbar Pain Relief PatchLumbar Pain Relief Patch

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1997510camphor 0.5 % / menthol 2.5 % Medicated PatchPSN1
1997510camphor 0.005 MG/MG / menthol 0.025 MG/MG Medicated PatchSCD1
1997510camphor 0.5 % / menthol 2.5 % Medicated PatchSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83713-002-122024-07-30C16284748780-11030e365-0827-111a-e063-dadaa90a10e2Lumbar Pain Relief Patch 83713-002-12
83713-002-122024-01-30C16284748780-11030e365-0827-111a-e063-dadaa90a10e2Lumbar Pain Relief Patch 83713-002-12

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83713-002-11Lumbar Pain Relief Patch2.1 g in 1 PATCHPATCH2.11
83713-002-12Lumbar Pain Relief Patch12 in 1 BAGPATCH121

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83713-002LUMBAR PAIN RELIEF PATCH (MENTHOL, CAMPHOR) PATCH [GUANGZHOU HONGBOYUAN TRADING CO., LTD.]12 package rows20231013_0782c8ff-36e8-f0ac-e063-6294a90aa87b.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83713-00283713-002-11, 83713-002-12

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
MYRRHJC71GJ1F3LIACT
SAFFLOWER4VBL71TY4YIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
MENTHOLL7T10EIP3AACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
07831e0d-c839-7153-e063-6394a90a8b7a0782c8ff-36e8-f0ac-e063-6294a90aa87b2023-10-12WarningsExact identifier
spl id: 07831e0d-c839-7153-e063-6394a90a8b7a
spl set id: 0782c8ff-36e8-f0ac-e063-6294a90aa87b

Reported adverse events (FAERS/openFDA)#

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