Chun Gi So

Manufacturer
CHO WELL GF
Effective date
2019-11-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:01:32

Label at a glance#

ProductChun Gi So
Active ingredientMENTHOL, CAMPHOR (NATURAL)
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

camphor, menthol

INACTIVE INGREDIENT SECTION

ledum palustre extract, ginger extract, angelica gigas extract, etc

OTC - PURPOSE SECTION

temporary relief of minor aches and pains of muscles and joints

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

apply it on body parts, for arms or legs, apply it on both sides together, and you can have better thermo-therapeutical effect

WARNINGS SECTION

do not use if you have red rash, swell, itch, or any other abnormal physical symptoms while applying it on your body parts

do not use it on injured body parts, eczema, or dermatitis

keep it at a room temperature and out of children's reach

be careful not to get it in your eyes

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1365000camphor 1 % / menthol 1 % Topical CreamPSN1
1365000camphor 10 MG/ML / menthol 10 MG/ML Topical CreamSCD1
1365000camphor 1 % / menthol 1 % Topical CreamSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73426-0001-12021-01-29C16284748780-1ba0f9c33-531e-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73426-0001-1Chun Gi So100 g in 1 PACKAGECREAM1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73426-0001CHUN GI SO (CAMPHOR, MENTHOL) CREAM [CHO WELL GF]1Legacy NDC, 1 package rows20191118_978788d1-64ea-0cb9-e053-2a95a90a23e8.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73426-000173426-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
978788f5-2310-4460-e053-2a95a90ab57a978788d1-64ea-0cb9-e053-2a95a90a23e82019-11-17WarningsExact identifier
spl id: 978788f5-2310-4460-e053-2a95a90ab57a
spl set id: 978788d1-64ea-0cb9-e053-2a95a90a23e8

Reported adverse events (FAERS/openFDA)#

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