FDA.reportPublic FDA data

Magictop Pain Relief Patch

Manufacturer
Zunyi Jici Bio-Health Products Co Ltd
Effective date
2018-12-28
Label type
HUMAN OTC DRUG LABEL
Version
32489
Source
full-release
Hydrated at
2026-05-31 22:58:00

Label at a glance#

ProductMagictop Pain Relief Patch
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL
Label structure14 sections

Indications and uses

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

Dosage and administration

Adults (12 years and older) - Clean and dry the affected area. - Peel film off from patch and apply the herbal formula side onto skin. - Lasts for up to 24 hours; repeat as necessary and no less than 2 hours between applications. - For the best result, a 2-week course of treatment is recommended. - Children under 12 years: Consult your physician.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor    1.6%
Menthol     2.0%

Purpose

OTC - PURPOSE SECTION

Camphor          Topical Analgesic
Menthol           Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY

Ask a Doctor or Pharmacist Before Use If You Are

OTC - ASK DOCTOR/PHARMACIST SECTION

pregnant.
lactating women.

When Using This Product

OTC - WHEN USING SECTION

Do not apply to wounds or damaged, broken or irritated skin.

Stop Use and Ask a Doctor If

OTC - STOP USE SECTION

condition worsens.
redness is present.
irritation develops.
symptoms persist for more than 7 days or clear up and occur again within a few days.

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 (12 years and older)
- Clean and dry the affected area.
- Peel film off from patch and apply the herbal formula side onto skin.
- Lasts for up to 24 hours; repeat as necessary and no less than 2 hours between applications.
- For the best result, a 2-week course of treatment is recommended.
- Children under 12 years: Consult your physician.

Other Information

OTHER SAFETY INFORMATION

Keep pouch sealed and avoid storage in direct sunlight.

Questions or Comments?

OTC - QUESTIONS SECTION

Magic Top Corp
16961 E Gale Ave, City of Industry, CA91745, USA
Tel: (626) 862-6809   Fax: (626)261-0925   www.magictop.net

Inactive Ingredients

INACTIVE INGREDIENT SECTION

LYCOPODIUM CLAVATUM WHOLE, IMPATIENS BALSAMINA WHOLE， FRANKINCENSE, MYRRH, CLEMATIS CHINENSIS ROOT, CYNANCHUM PANICULATUM WHOLE, BORNEOL, CAPSICUM OLEORESIN, LAUROCAPRAM

Distribted by

SPL UNCLASSIFIED SECTION

Magic Top Corp
16961 E Gale Ave, City of Industry, CA91745, USA
(626) 862-6809

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2107312camphor 1.6 % / menthol 2 % Medicated PatchPSN32489
2107312camphor 0.016 MG/MG / menthol 0.02 MG/MG Medicated PatchSCD32489
2107312camphor 1.6 % / menthol 2 % Medicated PatchSY32489

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72584-001-032021-01-29C16284748780-1ba0f9c33-3867-a910-e053-dadaa90a0b85Zunyi Jici Bio-Health Products Co Ltd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72584-001-01Magictop Pain Relief Patch20 g in 1 PATCHPATCH2032489
72584-001-02Magictop Pain Relief Patch3 in 1 BOXPATCH332489
72584-001-03Magictop Pain Relief Patch3 in 1 BOXPATCH332489

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72584-001MAGICTOP PAIN RELIEF PATCH (CAMPHOR, MENTHOL) PATCH [ZUNYI JICI BIO-HEALTH PRODUCTS CO LTD]32489Legacy NDC, 3 package rows20181229_cf89efcc-9ecf-4415-9bb5-2d538f72ee30.zip

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72584-00172584-001-01, 72584-001-02, 72584-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
MENTHOLL7T10EIP3AACTIB
LYCOPODIUM CLAVATUM WHOLE005ICF6L27IACT
IMPATIENS BALSAMINA WHOLEZMK32KX641IACT
FRANKINCENSER9XLF1R1WMIACT
MYRRHJC71GJ1F3LIACT
CLEMATIS CHINENSIS ROOT8Z18N528CUIACT
CYNANCHUM PANICULATUM WHOLET14ONG8D7HIACT
BORNEOLM89NIB437XIACT
CAPSICUM OLEORESINUW86K581WYIACT
LAUROCAPRAM1F3X9DRV9XIACT

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
738404aa-7c4f-4996-af4d-3a985a9b4318cf89efcc-9ecf-4415-9bb5-2d538f72ee302018-12-28WarningsExact identifier
spl id: 738404aa-7c4f-4996-af4d-3a985a9b4318
spl set id: cf89efcc-9ecf-4415-9bb5-2d538f72ee30

Reported adverse events (FAERS/openFDA)#

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