FDA.reportPublic FDA data

Magic For Pain Relief

Manufacturer
Zhuhai Aofute Medical Technology Co, Ltd
Effective date
2020-12-07
Label type
HUMAN OTC DRUG LABEL
Version
32707
Source
full-release
Hydrated at
2026-05-31 23:34:49

Label at a glance#

ProductMagic For Pain Relief
Active ingredientCAMPHOR (SYNTHETIC), METHYL SALICYLATE, MENTHOL
Label structure11 sections

Indications and uses

Temporarily relieves minor aches and pains of muscles and joints due to: simple backaches, arthritis, strains, bruises, sprains

Dosage and administration

Adults and children 2 years of age and older: spray medicated oil to the affected area, quickly cover and press it tightly until it gets hot, then release your hand, 1 to 3 times daily. Children under 2 years of age: Do not use, consult your physician.

Storage and handling

Keep container tightly closed. Store at 16 to 30°C (69 to 86°F) and keep away from direct sunlight.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Camphor 10%

Methyl Salicylate 30%

Menthol 16%

Purpose

OTC - PURPOSE SECTION

Camphor       External Analgesic

Methyl Salicylate     External Analgesic

Menthol         External Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporarily relieves minor aches and pains of muscles and joints due to: simple backaches, arthritis, strains, bruises, sprains

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: spray medicated oil to the affected area, quickly cover and press it tightly until it gets hot, then release your hand, 1 to 3 times daily. Children under 2 years of age: Do not use, consult your physician.

Warnings

WARNINGS SECTION

For external use only. Do not use on wounds, irritated or damaged skin, otherwise than as directed.

When Using This Product

OTC - WHEN USING SECTION

Avod contact with the eyes or mucous membranes. Do not bandage tightly.

Stop Use and Ask a Doctor If

OTC - STOP USE SECTION

Condition worsens

Symptoms persist for more than 7 days

Symptoms clear up and occur again within a few days

Excessive irritation of the skin develops

Nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs

When using for pain of arthritis: pain persists for more than 10 days, redness is present, in conditions affecting children 12 years of age.

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental poisoning. If swallowed, get medical help or contact Poison Control Center right away.

Other Information

STORAGE AND HANDLING SECTION

Keep container tightly closed. Store at 16 to 30°C (69 to 86°F) and keep away from direct sunlight.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

CARTHAMUS TINCTORIUS WHOLE, CAPSICUM ANNUUM WHOLE, PANAX NOTOGINSENG ROOT, REHMANNIA GLUTINOSA ROOT, ANGELICA PUBESCENS ROOT, DAEMONOROPS DRACO WHOLE, VANILLYL BUTYL ETHER, MUSCONE, BORNEOL, ALCOHOL

Drug Facts

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug FactsDrug Facts

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1941591menthol 16 % / methyl salicylate 30 % / synthetic camphor 10 % Topical SprayPSN32707
1941591menthol 160 MG/ML / methyl salicylate 300 MG/ML / synthetic camphor 100 MG/ML Topical SpraySCD32707
1941591menthol 16 % / methyl salicylate 30 % / synthetic camphor 10 % Topical SpraySY32707

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71419-001-012022-01-28C16284748780-1d6a99b39-b463-a426-e053-dadaa90af4c2Zhuhai Aofute Medical Technology Co, Ltd

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71419-001-01Magic For Pain Relief30 mL in 1 BOTTLE, PLASTICSPRAY3032707
71419-001-01Magic For Pain Relief1 in 1 BOXSPRAY132707

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71419-001MAGIC FOR PAIN RELIEF (CAMPHOR, METHYL SALICYLATE, MENTHOL) SPRAY [ZHUHAI AOFUTE MEDICAL TECHNOLOGY CO, LTD]32707Legacy NDC, 2 package rows20201209_e468d84e-9469-4d9a-8f95-a2fb9c893e2f.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71419-00171419-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
METHYL SALICYLATELAV5U5022YACTIB
MENTHOLL7T10EIP3AACTIB
CARTHAMUS TINCTORIUS WHOLE5EMV416J82IACT
CAPSICUM ANNUUM WHOLE7FKZ3QQQ1FIACT
PANAX NOTOGINSENG ROOTGQX1C1175UIACT
REHMANNIA GLUTINOSA ROOT1BEM3U6LQQIACT
ANGELICA PUBESCENS ROOT0MF1EI01KJIACT
DAEMONOROPS DRACO WHOLE1C8HA8O22CIACT
VANILLYL BUTYL ETHERS2ULN37C9RIACT
MUSCONEUPS3C6CV36IACT
BORNEOLM89NIB437XIACT
ALCOHOL3K9958V90MIACT

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
0ebedb2a-50d0-4204-ad19-2b3c318ba141e468d84e-9469-4d9a-8f95-a2fb9c893e2f2020-12-07WarningsExact identifier
spl id: 0ebedb2a-50d0-4204-ad19-2b3c318ba141
spl set id: e468d84e-9469-4d9a-8f95-a2fb9c893e2f

Reported adverse events (FAERS/openFDA)#

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