HOT PAIN RELIEF

Manufacturer
Suzhou Vastech Medical Technology Co., Ltd
Effective date
2017-06-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:51:46

Label at a glance#

ProductHOT PAIN RELIEF
Active ingredientCAPSAICIN
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients Purpose

Capsicum Extract Capsaicin 0.025%..............................Topical Analgesic

OTC - PURPOSE SECTION

Uses

For temporary relief associated with:

  • Arthritis
  • Backaches
  • Bruises
  • Sprains & Strains
  • Joint & Muscle Pain

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use:

  • On the face or rashes
  • With a heating pad
  • On wounds or damaged skin
  • if you are allergic to any ingredients of this product

OTC - WHEN USING SECTION

When using this product:

  • Use only as directed
  • Avoid contact with the eyes, mucous membranes or rashes

OTC - STOP USE SECTION

Stop use and ask a doctor if:

  • Rash, itching or excessive skin irritation develops
  • Conditions worsen
  • Symptoms persist for more than 7 days
  • Symptoms clear up and occur again within a few days

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poision Control Center right away.

INDICATIONS & USAGE SECTION

Directions

Adults and Children 12 years of age and over:

Clean and dry affected area.
Peel off protective film and apply patch once or twice a day.
Apply patch an hour after and before shower or bath. Patch will remain effective for 8 hours.

Children Under 12 Years of Age: Consult a physician.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Belladonna extract, camphor, diphenhydramine, lanolin, peppermint oil, rubber, vaseline, methyl salicylate, polyster resin, zinc oxide

DOSAGE & ADMINISTRATION SECTION

Distributed by:

MCURE HEALTH SOLUTIONS INC.

20819 Currier Rd #200

City of Industry, CA 91789

MADE IN CHINA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PA-200PA-200

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0e2e0f88-b076-afe1-4bdd-32bca4375becProduct name320250127
473d070d-1c38-488e-b991-c4d1bf45aab8Product name120210201
3e48c9c4-918d-5d23-2f0b-d2398b06be54Product name120140508
865c72dd-0d94-daac-f728-ddd4ded2a79eProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71183-002-252020-01-31C16284748780-19d75b9d0-32fe-f424-e053-dadaa90a57ce530e42a3-a5d9-1c49-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71183-002-25HOT PAIN RELIEF4800 mg in 1 PATCHPATCH48001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71183-002HOT PAIN RELIEF (CAPSAICIN PATCH) PATCH [SUZHOU VASTECH MEDICAL TECHNOLOGY CO., LTD]1Legacy NDC, 1 package rows20170629_530e42a3-a5d9-1c49-e054-00144ff88e88.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71183-00271183-002-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
530e42a3-a5da-1c49-e054-00144ff88e88530e42a3-a5d9-1c49-e054-00144ff88e882017-06-28WarningsExact identifier
spl id: 530e42a3-a5da-1c49-e054-00144ff88e88
spl set id: 530e42a3-a5d9-1c49-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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