Therapain Plus

Manufacturer
Epic Laboratories, LLC
Effective date
2026-03-02
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:48:30

Label at a glance#

ProductTherapain Plus
Active ingredientMENTHOL
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Natural L-menthol 2%

OTC - PURPOSE SECTION

Purpose

Topical Analgesic

INDICATIONS & USAGE SECTION

Uses:

Relieves temporary pains due to:

  • Arthritis ​
  • Stiffness
  • Sprains and Strains
  • Neck and barckaches
  • Muscle Soreness
  • Cramps

WARNINGS SECTION

Warnings:

FOR EXTERNAL USE ONLY

WARNINGS AND PRECAUTIONS SECTION

Flammable, Avoid

  • heat
  • sparks
  • open flame

When using this product

  • Avoid contact with eyes, mouth, genitalia, mucous membrane, irritated and very sensitive skin
  • Do not apply to open wounds or damaged skin.
  • Do not bandage tightly.
  • Do not. use if you are diabetic or have impaired circulation

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • Excessive skin irritation develops
  • Condition worsens.
  • Symptoms persist more than 7 days, discontinue use of this product and consult a doctor

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION SECTION

Directions:

  • Shake well
  • Roll-on liberally to affected area not more than 3 to 4 times daily. Wash hands with soap and water after applying.
  • Children under 12years of age: consult a physician.
  • After first coat absorbs into skin, re-apply 1-3 extra coats to increase effectiveness.
  • Formula dries quickly and won't stain clothes or leave skin lingering with an unplesant medicine scent.

INACTIVE INGREDIENT SECTION

Other ingredients

Deionized Water, Isopropyl Alcohol, Methyl Sulfonyl Methane (MSM)**,

Glucosamine Sulfate**, Oil of Peppermint, Oil of Eucalyptus,

**For Use as a Skin Conditioner

OTC - QUESTIONS SECTION

Questions or Comments:

Call toll free: 800-667-1969

Relief-Mart, Inc.

28505 Canwood St. Ste. C

Agoura Hills, CA 93101

www.TherapainPlus.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Roll-OnRoll-On

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1146695menthol 2 % Topical SolutionPSN5
1146695menthol 20 MG/ML Topical SolutionSCD5
1146695menthol 2 % Topical SolutionSY5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58418-827-032024-08-22C16284748780-11030e365-340e-111a-e063-dadaa90a10e2Therapain Plus Roll On
58418-827-032024-07-30C16284748780-11030e365-340e-111a-e063-dadaa90a10e2Therapain Plus Roll On
58418-827-032024-01-30C16284748780-11030e365-340e-111a-e063-dadaa90a10e2Therapain Plus Roll On

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58418-827-03Therapain Plus88.5 mL in 1 BOTTLE, DISPENSINGLIQUID88.55

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
58418-82758418-827-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
Therapain PlusMENTHOL ROLL-ONEpic Laboratories, LLC0249cfdf-b7c4-f27d-e063-6294a90aaa262026-03-02WarningsExact identifier
ndc (package): 58418-827-03
ndc (product): 58418-827
ndc11 (package): 58418082703
spl id: 4c12906d-43bf-553f-e063-6394a90a6edd
spl set id: 0249cfdf-b7c4-f27d-e063-6294a90aaa26

Reported adverse events (FAERS/openFDA)#

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