87786-022

Manufacturer
Wenzhou Yuyuan Pharmaceutical Co., Ltd.
Effective date
2026-07-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-21 05:10:24

Label at a glance#

ProductDRAVYNOR TOPICAL ANALGESIC HEAT Patch
Active ingredientMENTHOL, CAPSAICIN
Label structure12 sections

Dosage and administration

adults and children over 12 years. remove backing from patch by firmly grasping both ends and gently pulling until backing separates in middle carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area once exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected area Wear one patch for up to 8 hours. Repeat if ...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 24mg Capsaicin 16mg

Purpose

OTC - PURPOSE SECTION

Patch Topical Analgesic

Use

INDICATIONS & USAGE SECTION

■ temporarily relieves minor pain associated with:
■ arthritis ■ simple backache ■ bursitis ■ tendonitis ■ muscle strains ■ sprains ■ bruises ■ cramps

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

with a heating pad or any additional external heat source.

When Using

OTC - WHEN USING SECTION

■ Use only as directed. Read and follow all directions and warnings on this carton.
■ Avoid contact with eyes and mucous membranes
■ Do not apply to wounds or damaged skin, broken or irritated skin
■ A transient burning sensation may occur upon application but usually disappears within a few days.

Stop Use

OTC - STOP USE SECTION

■ condition worsens
■ redness is present
■ irritation develops
■ symptoms persist for more than 7 days or clear up and occur again within a few days

Ask Doctor

OTC - ASK DOCTOR SECTION

■ condition worsens
■ redness is present
■ irritation develops
■ symptoms persist for more than 7 days or clear up and occur again within a few days

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

adults and children over 12 years.
remove backing from patch by firmly grasping both ends and gently pulling until backing separates in middle
carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area
once exposed portion of patch is positioned, carefully remove remaining backing to completely apply patch to affected area
Wear one patch for up to 8 hours.
Repeat if needed, but do not use more than 3 times daily.
children 12 years or younger: ask a doctor

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin,Sodium Polyacrylate, Sodium Carboxymethyl Cellulose, Dihydroxyaluminum Aminoacetate, Titanium Dioxide, Tetrasodium EDTA, Purified Water, Tartaric Acid

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

24mg 16mg24mg 16mg

Products#

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DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87786-02287786-022-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
DRAVYNOR TOPICAL ANALGESIC HEAT PatchMENTHOL 24MG CAPSAICIN 16MG TOPICAL ANALGESIC HEAT PATCHWenzhou Yuyuan Pharmaceutical Co., Ltd.56b83ee8-8d86-9436-e063-6294a90a0c252026-07-16WarningsExact identifier
ndc (package): 87786-022-01
ndc (product): 87786-022
ndc11 (package): 87786002201
spl id: 56b83ee8-8d87-9436-e063-6294a90a0c25
spl set id: 56b83ee8-8d86-9436-e063-6294a90a0c25

Reported adverse events (FAERS/openFDA)#

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