FDA.reportPublic FDA data

DRMITSUI Pain Relieving Patch

Manufacturer
Guangzhou Ruyu Cosmetics Co., Ltd
Effective date
2025-12-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:25:42

Label at a glance#

ProductDRMITSUI Pain Relieving Patch
Active ingredientMENTHOL, CAMPHOR, (-)-, METHYL SALICYLATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVEINGREDIENTS
PURPOSE
CamphorMenthol
3.1%
Topical analgesicTopical analgesicTopical analgesic
6.0%
Methyl salicylate 10.0%

OTC - PURPOSE SECTION

For temporary relief of minor aches & pains of muscles & joints associated with:Arthritis, Simple backache, Strains, Bruises, Sprains

INACTIVE INGREDIENT SECTION

MINERAL OIL, PERFUME,POLYISOBUTYLENE, STYRENE-ISOPRENE-STYRENE BLOCK COPOLYMER.
SYNTHETIC ALUMINUM SILICATE,TERPENE RESIN, TITANIUM DIOXIDE.

WARNINGS SECTION

1.For external use only.
2.Allergy alert: lf prone to allergic reaction from aspirin or salicylates, consult a doctor before use3.Do not use: On wounds or damaged skin. With a heating pad. lf you are allergic to anyingredients of this product.
4.When using this product: Use only as directed. Avoid contact with the eyes. mucousmembranes or rashes. Do not bandage tightly
5.Stop using it and ask a doctor if: Skin reactions such as redness, itching, rash, excessiveirritation, burning sensation,swelling or blistering occur. Conditions worsen.Symptomspersist for more than 7 days. Symptoms clear up and occur again within a few days6.Pregnancy/breast-feeding warning: lf pregnant or breast-feeding, ask a healthprofessional before use.

DOSAGE & ADMINISTRATION SECTION

Apply to affected areas not morethan 3 to 4 times daily.

Remove patch from the skin after at most 8-hour application.

INDICATIONS & USAGE SECTION

DIRECTIONS
Adults and children 12 years of age and over:1. Clean and dry affected area. 2. Remove patch from film. 3. Apply to affected areas not morethan 3 to 4 times daily. 4. Remove patch from the skin after at most 8-hour application.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of children to reach

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85713-101-01DRMITSUI Pain Relieving Patch10 g in 1 PATCHPATCH101
85713-101-01DRMITSUI Pain Relieving Patch6 in 1 BOXPATCH61

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85713-10185713-101-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
CAMPHOR, (-)-213N3S8275ACTIB
MINERAL OILT5L8T28FGPIACT
POLYISOBUTYLENE 35-39TQ77WR8A02IACT
ALUMINUM SILICATET1FAD4SS2MIACT
TERPENE RESINGR35AH6YDNIACT
STYRENE/ISOPRENE/STYRENE BLOCK COPOLYMERK7S96QM8DVIACT
METHYL SALICYLATELAV5U5022YACTIB

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
460c376c-3027-2460-e063-6394a90a0089460c376c-3026-2460-e063-6394a90a00892025-12-16WarningsExact identifier
spl id: 460c376c-3027-2460-e063-6394a90a0089
spl set id: 460c376c-3026-2460-e063-6394a90a0089

Reported adverse events (FAERS/openFDA)#

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