EXTERNAL ANALGESIC PATCH

Manufacturer
Zhengzhou Daohe Medical Technology Co.,Ltd
Effective date
2023-12-26
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:05:41

Label at a glance#

ProductEXTERNAL ANALGESIC
Active ingredientCAMPHOR (SYNTHETIC), CAPSICUM, MENTHOL
Label structure6 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache  arthritis strains bruises sprains

Dosage and administration

Adults and children 12 years of age and older: Clean and dry affected area. Remove from backing film and apply. Remove from the skin after at most 8 hour's application Apply to the affected area not more than 3 times daily. Children under 12 years of age: Consult a doctor.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 9.6%

Capsicum containing 0.05% Capsaicin

Menthol 7.8%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with

  • simple backache 
  • arthritis
  • strains
  • bruises
  • sprains

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes
  • do not apply to wounds or damaged skin 
  • do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • if symptoms persist for more than 7 days or clear up and occur again within a few days

If pregnant or breast-feeding, 

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Adults and children 12 years of age and older:
  • Clean and dry affected area.
  • Remove from backing film and apply.
  • Remove from the skin after at most 8 hour's application
  • Apply to the affected area not more than 3 times daily.
  • Children under 12 years of age: Consult a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylic Acid, Aluminum Hydroxide, Carmellose Sodium 2-Ethylhexylacrylate, Glycerin, Methyl Acrylate, Polyacrylate, Polyacrylic Acid, Sodium Polyacrylate, Tartaric Acid, Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1807136camphor 9.6 % / capsaicin 0.05 % / menthol 7.8 % Medicated PatchPSN3
1807136camphor 0.096 MG/MG / capsaicin 0.0005 MG/MG / menthol 0.078 MG/MG Medicated PatchSCD3
1807136camphor 9.6 % / capsaicin 0.05 % / menthol 7.8 % Medicated PatchSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
CAPSICUM Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73567-001-002025-01-30C16284748780-12cef2736-7809-d83d-e063-dadaa90ab31fEXTERNAL ANALGESIC PATCH

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73567-001-00EXTERNAL ANALGESIC8 mL in 1 PATCHPATCH83
73567-001-00EXTERNAL ANALGESIC1 in 1 POUCHPATCH13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73567-001EXTERNAL ANALGESIC (CAMPHOR (SYNTHETIC), CAPSICUM, MENTHOL) PATCH [ZHENGZHOU DAOHE MEDICAL TECHNOLOGY CO.,LTD]3Legacy NDC, 2 package rows20231227_36cb2580-db8f-4926-b498-ae4a074cd576.zip

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
73567-00173567-001-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
0d773c0d-7a28-d567-e063-6394a90a9c5436cb2580-db8f-4926-b498-ae4a074cd5762023-12-26WarningsExact identifier
spl id: 0d773c0d-7a28-d567-e063-6394a90a9c54
spl set id: 36cb2580-db8f-4926-b498-ae4a074cd576

Reported adverse events (FAERS/openFDA)#

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