FDA.reportPublic FDA data

HYSAN ANALGESIC

Manufacturer
HYSAN PHARMACEUTICAL CO LTD
Effective date
2024-10-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:22:45

Label at a glance#

ProductHYSAN ANALGESIC
Active ingredientMETHYL SALICYLATE, CAMPHOR (SYNTHETIC)
Label structure14 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Drug Facts

Active Ingredients

Methyl Salicylate 22%

Camphor 2%

OTC - PURPOSE SECTION

Purpose

External Analgesic

INDICATIONS & USAGE SECTION

Uses

Temporarily relieves minor aches, pains of muscles and joint pains due to:

  • simple backache
  • arthritis
  • strains
  • sprains
  • bruises

WARNINGS SECTION

Warnings

  • external use only
  • use only as directed

OTC - DO NOT USE SECTION

Do not use

  • on opened wounds
  • on damaged skin

OTC - WHEN USING SECTION

When using this product

  • avoid contact with the eyes
  • do not banage tighly

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • a rash or irritation develops
  • condition worsens
  • symptoms persist for more than 7 days or clears 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 to avoid accidental poisoning. If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

Directions

  • adults and children 12 years and older, apply appropriate amount to the affected area. Apply pressure and massage gently not more than 3 to 4 times daily
  • children under 12 years of age, consult a doctor before using

OTHER SAFETY INFORMATION

Other Information

  • Be stored below 28°C (82°F)
  • Closed tightly after used

INACTIVE INGREDIENT SECTION

Inactive ingredients

eucalyptus Oil, menthol, paraffin

OTC - QUESTIONS SECTION

Questions or comments?

(626) 354 1819 M-F 9am to 5pm

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hysan_AO_MIC_2021Hysan_AO_MIC_2021

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1791346camphor 2 % / methyl salicylate 22 % Topical OintmentPSN2
1791346camphor 0.02 MG/MG / methyl salicylate 0.22 MG/MG Topical OintmentSCD2
1791346camphor 2 % / methyl salicylate 22 % Topical OintmentSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63255-330-01HYSAN ANALGESIC75 g in 1 JAROINTMENT752

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63255-330HYSAN ANALGESIC (METHYL SALICYLATE, CAMPHOR (SYNTHETIC)) OINTMENT [HYSAN PHARMACEUTICAL CO LTD]2Current NDC, Legacy NDC, 1 package rows20241006_99a13b0a-1d77-479e-ba99-2cfa638de339.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63255-33063255-330-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
METHYL SALICYLATELAV5U5022YACTIB
CAMPHOR (SYNTHETIC)5TJD82A1ETACTIB
EUCALYPTUS OIL2R04ONI662IACT
MENTHOLL7T10EIP3AIACT
PARAFFINI9O0E3H2ZEIACT

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
HYSAN ANALGESICMETHYL SALICYLATE, CAMPHOR (SYNTHETIC)HYSAN PHARMACEUTICAL CO LTD99a13b0a-1d77-479e-ba99-2cfa638de3392024-10-04WarningsExact identifier
ndc (package): 63255-330-01
ndc (product): 63255-330
ndc11 (package): 63255033001
spl id: 3924cc39-221a-4f6d-b62f-394dffa8874d
spl set id: 99a13b0a-1d77-479e-ba99-2cfa638de339

Reported adverse events (FAERS/openFDA)#

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