Cellapy Pure Derma Sanitizer

Manufacturer
GM Holdings Co., Ltd | Ester Co., Ltd.
Effective date
2020-04-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:05:36

Label at a glance#

ProductCellapy Pure Derma Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Uses : Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available

Dosage and administration

Directions: • Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 years of age when using this product to avoid swallowing.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: Ethyl Alcohol 76% v/v

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT:

Water, Butylene Glycol, Carbomer, Triethanolamine, Aloe Barbadensis Leaf Extract, Polyoxyethylene Hydrogenated Castor oil, Fragrance

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: Antiseptic

WARNINGS

WARNINGS SECTION

Warnings:


For external use only. Flammable. Keep away from heat or flame


Do not use
in children less than 2 months of age
on open skin wounds


When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.


Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.


Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Uses:

INDICATIONS & USAGE SECTION

Uses :

Hand sanitizer to help reduce bacteria that potentially can cause disease.
For use when soap and water are not available

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

OTHER SAFETY INFORMATION

Other information:
• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69278-112-012022-01-28C16284748780-1d6a99b39-bd69-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69278-112-01Cellapy Pure Derma Sanitizer500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69278-112CELLAPY PURE DERMA SANITIZER (ALCOHOL) GEL [GM HOLDINGS CO., LTD]1Legacy NDC, 1 package rows20200410_43bcbb53-425d-46e4-b660-e3925971c4dd.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69278-11269278-112-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
66db53dc-9818-43e1-a10a-4e0b1a6206d543bcbb53-425d-46e4-b660-e3925971c4dd2020-04-10WarningsExact identifier
spl id: 66db53dc-9818-43e1-a10a-4e0b1a6206d5
spl set id: 43bcbb53-425d-46e4-b660-e3925971c4dd

Reported adverse events (FAERS/openFDA)#

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