Pain Relieving Patch

Manufacturer
Heilongjiang Huashen Science & Technology Development Co Ltd
Effective date
2010-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:23:27

Label at a glance#

ProductPain Relieving Patch
Active ingredientMENTHOL
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient ( in each patch)               Purpose

Menthol 0.2 percent                                       Analgesic

OTC - PURPOSE SECTION


Uses:
For the temporary relief of pain.

WARNINGS SECTION

Warnings:

For external use only. Avoid contact with the eyes.

If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again

within a few days, discontinue use of this product and consult a doctor.

OTC - DO NOT USE SECTION


Do not use

- otherwise than as directed

- in the eyes or ears

- if you are pregnant

- if you have skin allergy or damage to skin

OTC - STOP USE SECTION

Stop use and ask a doctor if

- redness is present

- excessive irritation of the skin develops

- side effects occur. You may report side effects to FDA at 1-800-FDA-1088

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep  out of reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions:

Adults and children 2 years of age and older:  Remove patch from package. Apply to affected area not more than 3-4 times daily. Leave bandage

                                                                                  on for no more than 48 hours.


Children under 2 years of age: Consult a doctor.

DESCRIPTION SECTION

Manufactured by:

Heilongjiang Huashen Science and Technology

Development Co. Ltd. China

Investment Building, No.235 HongQi Street,

High and New Technology Development Zone,

Harbin, HeilLongjiang Province, China

86 451 82262828

hs huashen.net

www.huashen.net

Product of China

Distributed By:

Exclusive Representation Center of

Huashen Corporation

1635 Bath Ave

Brooklyn, NY 11214

718 841 7770

www planethuashen com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HuaShen Pain Relieving Patch

Continuous Relief for up to

48

hours

- fast

- effective

- natural

5 Adhesive Patches with Menthol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HuashenPainRelievingPatchHuashenPainRelievingPatch

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1793231menthol 0.2 % Medicated PatchPSN1
1793231menthol 0.002 MG/MG Medicated PatchSCD1
1793231menthol 0.2 % Medicated PatchSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50309-777-152019-10-21C16284748780-1956f9ecf-d8db-621f-e053-dbdaa90a74adPain Relieving Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50309-777-15Pain Relieving Patch5 in 1 PACKAGEPATCH51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50309-777PAIN RELIEVING PATCH (MENTHOL) PATCH [HEILONGJIANG HUASHEN SCIENCE & TECHNOLOGY DEVELOPMENT CO LTD ]1Legacy NDC, 1 package rows20100130_72be6046-c92f-4a3a-9f7e-a80b3fbff410.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
MENTHOLACTIVE INGREDIENTL7T10EIP3A1
MENTHOLACTIVE MOIETYL7T10EIP3A1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50309-77750309-777-15

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
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
8d0e5e63-2766-4a91-98a7-a4e203a1a6f572be6046-c92f-4a3a-9f7e-a80b3fbff4102010-01-08WarningsExact identifier
spl id: 8d0e5e63-2766-4a91-98a7-a4e203a1a6f5
spl set id: 72be6046-c92f-4a3a-9f7e-a80b3fbff410

Reported adverse events (FAERS/openFDA)#

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