Dr Tans Arthritis Formula 3 day Patch

Manufacturer
Great Loong LLC | Tianjin Ruide Pharmaceutical Co., Ltd.
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:46:40

Label at a glance#

ProductDr Tans Arthritis Formula 3 day Patch
Active ingredientMENTHOL
Label structure8 sections

Dosage and administration

Clean and dry the affected area. Peel film off of patch and apply the herbal-formula side onto the skin. Peel film off the larger dressing patch and apply over the herbal patch to secure it in place. Patch will continue to release herbal formula to the skin for 3 days if desired.

Label contents#

Full prescribing information#

Actives

OTC - ACTIVE INGREDIENT SECTION

Menthol 0.5 %

Inactives

INACTIVE INGREDIENT SECTION

Borneol , Carthamus Tinctorious L. , Draconis Sanguis, Frankincense, Ligusticum Walichii, Padix Auklandiae, Radix Angelicae Forrnosanae, Radix Paeoniae Rubra, Rheum Officinale Baillon, Sandalwood, Syzygium Aromaticum, hydrogel.

Purpose

OTC - PURPOSE SECTION

External Analgesic

Indication and Usage

INDICATIONS & USAGE SECTION

For adults and children 10 and older for the temporary relief of: • chronic arthritis • backache • joint and muscle pain and stiffness • old sports injuries.

Directions 

DOSAGE & ADMINISTRATION SECTION

Clean and dry the affected area. Peel film off of patch and apply the herbal-formula side onto the skin. Peel film off the larger dressing patch and apply over the herbal patch to secure it in place. Patch will continue to release herbal formula to the skin for 3 days if desired.

Warnings

WARNINGS SECTION

• For external use only. • Do not apply to open sores or wounds. • If skin irritation or a rash occurs, remove patch and consult physician. ·Avoid contact with eyes and mucous membranes. • If pregnant or breast feeding, consult a doctor before using.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children 

Product label 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

artrhritisartrhritis

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71446-001-012024-01-30C16284748780-11030e365-2c02-111a-e063-dadaa90a10e2Dr Tans Arthritis Formula 3 day Patch

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71446-001-01Dr Tans Arthritis Formula 3 day Patch2 in 1 PACKAGEPATCH25
71446-001-01Dr Tans Arthritis Formula 3 day Patch0.5 g in 1 PATCHPATCH0.55

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71446-001DR TANS ARTHRITIS FORMULA 3 DAY PATCH (MENTHOL) PATCH [GREAT LOONG LLC]5Legacy NDC, 2 package rows20220114_24f892b3-5328-47fa-aa5c-48575ef1c368.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71446-00171446-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
d57d5f50-34c4-baae-e053-2a95a90a7d6d24f892b3-5328-47fa-aa5c-48575ef1c3682022-01-13WarningsExact identifier
spl id: d57d5f50-34c4-baae-e053-2a95a90a7d6d
spl set id: 24f892b3-5328-47fa-aa5c-48575ef1c368

Reported adverse events (FAERS/openFDA)#

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