Dr Demand Relief Pain Relief Cream

Manufacturer
Mind and Body Research Corp | VEGE-KURL, INC.
Effective date
2019-02-27
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 22:58:39

Label at a glance#

ProductDr Demand Relief Pain Relief
Active ingredientMETHYL SALICYLATE, CAPSAICIN, MENTHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose
Capsaicin (0.025%)..........External Analgesic
Menthol (10.o%).............External Analgesic
Methyl Salicylate (25%)...External Analgesic

OTC - PURPOSE SECTION

Uses
Temporary relief of minor aches & pains
of muscles & joints associated with:
• Simple Backaches • Arthritis • Strains
• Bruises • Sprains

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental ingestion. If
swallowed, get medical help or contact a Poison Control Center
immediately.

WARNINGS SECTION

Warnings
For external use only.
Do not use
• on wounds or damaged skin
• with heating pad
• on a child under 12 years of age with
arthritis like conditions
Ask a doctor before use if you have
redness over the affected area.
When using this product:
• avoid contact with mucous membranes
• do not bandage tightly

DOSAGE & ADMINISTRATION SECTION

Directions
• Use only as directed.
• Adults and children 12 years of age and older, apply to affected
area not more than 3 to 4 times daily.
• Children under 12 years of age, ask a doctor
• Wash hands after use.

INACTIVE INGREDIENT SECTION

Inactive Ingredients Water, Cetyl Alcohol, (Hemp)Seed Oil, Stearic Acid, Glyceryl Stearate, Propylene Glycol,
Egg Shell Membrane, PEG-100 Stearate, Dimethyl Sulfone, Lavendula Officinalis Flower Oil, Natural Extractives of Chillie
Peppers, Xanthan Gum, Triethanolamine, Phenoxyethanol, Ethylhexylglycerin, Arnica Montana Flower Extract.

INDICATIONS & USAGE SECTION

Stop use and ask a docter if
• condition worsens or symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days
• excessive skin irritation occurs

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dr Demand Relief

Pain Relief Cream

Developed with Propietary ingredients

demand relief tubedemand relief tube

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
282751capsaicin 0.025 % / menthol 10 % / methyl salicylate 25 % Topical CreamPSN5
282751capsaicin 0.25 MG/ML / menthol 100 MG/ML / methyl salicylate 250 MG/ML Topical CreamSCD5
282751capsaicin 0.025 % / menthol 10 % / methyl salicylate 25 % Topical CreamSY5

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72185-225-012021-01-29C16284748780-1ba0f9c33-4d66-a910-e053-dadaa90a0b85Dr Demand Relief Pain Relief Cream

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72185-225-01Dr Demand Relief Pain Relief71 g in 1 TUBECREAM715

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72185-225DR DEMAND RELIEF PAIN RELIEF (CAPSAICIN, MENTHOL, METHYL SALICYLATE) CREAM [MIND AND BODY RESEARCH CORP]5Legacy NDC, 1 package rows20190228_6626402b-dbab-05fb-e053-2991aa0a603a.zip

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72185-22572185-225-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 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
82e56b22-ae21-093a-e053-2991aa0a3aed6626402b-dbab-05fb-e053-2991aa0a603a2019-02-27WarningsExact identifier
spl id: 82e56b22-ae21-093a-e053-2991aa0a3aed
spl set id: 6626402b-dbab-05fb-e053-2991aa0a603a

Reported adverse events (FAERS/openFDA)#

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