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#
Contacts and useful links#
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
Product of China
Distributed By:
Exclusive Representation Center of
Huashen Corporation
1635 Bath Ave
Brooklyn, NY 11214
718 841 7770
www planethuashen comPACKAGE 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
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50309-777-15 | 2019-10-21 | C162847 | 48780-1 | 956f9ecf-d8db-621f-e053-dbdaa90a74ad | Pain Relieving Patch |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 50309-777-15 | Pain Relieving Patch | 5 in 1 PACKAGE | PATCH | 5 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| MENTHOL | ACTIVE INGREDIENT | L7T10EIP3A | 1 | |
| MENTHOL | ACTIVE MOIETY | L7T10EIP3A | 1 |
Products#
Every source-derived product name is available through these pages.
- Pain Relieving Patch
- MENTHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50309-777 | 50309-777-15 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| MENTHOL | L7T10EIP3A | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 8d0e5e63-2766-4a91-98a7-a4e203a1a6f5 | 72be6046-c92f-4a3a-9f7e-a80b3fbff410 | 2010-01-08 | Warnings | 8d0e5e63-2766-4a91-98a7-a4e203a1a6f5 72be6046-c92f-4a3a-9f7e-a80b3fbff410 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
