DoctorRelief

Manufacturer
Biotanico Inc.
Effective date
2018-03-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:00:38

Label at a glance#

ProductDoctorRelief
Active ingredientMenthol
Label structure12 sections

Storage and handling

 Store in cool dry place from directly sunlight  Re-seal package arter open

Label contents#

Full prescribing information#

Actives

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purpose
Menthol 50 mg patch............................................Topical analagesic

OTC - PURPOSE SECTION

Topical analgesic

Indication 

INDICATIONS & USAGE SECTION

Uses
Temporary relief minor aches and pains of muscles and joints associated with:
■Arthritis ■Bruises ■Simple backache ■Strains ■Sprains

Warnings

WARNINGS SECTION

For external use only
When using this product:
■ Use only as directed
■ Avoid contact with eyes ,mucous membranes or rashes
■ Do not apply to broken, wounded or damaged skin
■ Do not bandage or cover with any type of wrap except clothing
■ Do not use with a heating pad or apply external heat
■ Discontinue use at least 1 hour before a bath or shower and do not use immediately after a bath or shower

Questons

OTC - QUESTIONS SECTION

Stop use and ask a doctor if
■ Rash, itching or excessive skin irritation develops
■ Condition worsens or does not improve after regular use
■ Symptoms persist for more than 7 days or clear up and occur again within a few days

OTC-Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

**Keep out of reach of children**
If swallowed, get medical help or contact a Poison Control Center immediately

Dosages

DOSAGE & ADMINISTRATION SECTION

Directions
Adult and children 12 years of age and over
■ Clean and dry affected area
■ Open pouch and remove patch. If desired, cut patch to size
■ Peel off protective backing and apply sticky side to affected area
■ Apply to affected area not more than 3 times daily
■ Wash hands with soap after applying patch
Children under 12 years of age
■ Consult a doctor

Warning and Precautions

WARNINGS AND PRECAUTIONS SECTION

  • Do not apply on Ulcerative or suppurative skin area
  • Not be used by during pregnancy
  • This product may cause allergic reaction in some individuals.

Ask Doctor

OTC - ASK DOCTOR SECTION

  • Ask a doctor if symptoms persist for more than 7 days or clear up and occur again within a few days
  • Rash,itching,execessive skin irritation develop
  • condition worsen or dose not improve after regular use

Inactives

INACTIVE INGREDIENT SECTION

Rosin,Rinus(Ricinus communis),zinc oxide,Clematis chinensis root,Bee'wax,Myrrh(calcined),Mastic(calcined),Cochinchina momordica seed, Methyl salicylate,Indigo carmine(F,D&C# Blue),F,D&C #Yellow and Q.S with sesame oil to 1g

Storage and handling section

  •  Store in cool dry place from directly sunlight
  •  Re-seal package arter open

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of DoctorRelief LabelImage of DoctorRelief LabelImage of DoctorRelief LabelImage of DoctorRelief Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
57842-7734-12025-12-02C16284748780-19d75b9d0-6976-f424-e053-dadaa90a57ceDoctorRelief
57842-7734-12020-01-31C16284748780-19d75b9d0-6976-f424-e053-dadaa90a57ceDoctorRelief

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57842-7734DOCTORRELIEF (MENTHOL) PATCH [BIOTANICO INC.]1Legacy NDC20180327_149b1382-5b3a-4390-9ce6-74cdbf3d3984.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57842-773457842-7734-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
dd2063a6-b3e3-4583-b960-daa2bf27d325149b1382-5b3a-4390-9ce6-74cdbf3d39842025-12-02WarningsExact identifier
spl set id: 149b1382-5b3a-4390-9ce6-74cdbf3d3984

Reported adverse events (FAERS/openFDA)#

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