Cellapy Dr Sanitizer

Manufacturer
GM Holdings Co., Ltd | Korea Life Science Co.,ltd
Effective date
2020-03-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:27

Label at a glance#

ProductCellapy Dr Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Uses : Externally disinfects the hands and skin

Dosage and administration

Directions: Pour a small amount onto hands, spready evenly and rub into skin

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: Ethanol (Synthetic Alcohol 70%)

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT:

Glycerin, Propylene Glycol, Carbomer, Camellia Sinesis Leaf Extract, Aloe Barbadensis Leaf Extract, Sodium Hyaluronate, Triethanolamine, Citrus Limon (Lemon) Fruit Oil, Water

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: Disinfecting Agent

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

Uses:

INDICATIONS & USAGE SECTION

Uses : Externally disinfects the hands and skin

WARNINGS

WARNINGS SECTION

Warnings
For external use only
When using this product if following abnormal symptoms persist, discontinue use
1) Irritation around the eyes, ears, mucous membranes, including the mouth, under the skin irritation and rashes

Stop immediately and consult a doctor if you experience
1) Hypersensitivity symptoms such as erythema, itching and dermatitis.
2) Skin Irritation
3) Following Instructions when using medication
a) For external use only (Do not use internally)
b) Avoid getting into the eyes
(if contact occurs, wash well with clean water)
Be careful to not inhale or use excessively for a long time (ingesting ethanol repeatedly causes irritation to mucous membranes and headaches or other symptoms may appear. When used repeatedly in the same area, skin irritation may occur.
Do not use the product for a long time in the same area as swelling, inflammation may occur or sickness due to absorption through the skin.
It is not recommended to use this one areas that have been medically treated with a cast or bandage.
Do not use in combination with soap or antibacterial cleansing agents.
Precautions
1) Keep out of open flames
2) Keep out of reach of children
3) Do not replace the container with another as quality deterioration or accidents may occur

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:
Pour a small amount onto hands, spready evenly and rub into skin

PACKAGE LABEL - 70mL Tube

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of tubeImage of tube

PACKAGE LABEL - 500mL Bottle Pump

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottleImage of bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69278-110-012022-01-28C16284748780-1d6a99b39-534c-a426-e053-dadaa90af4c2Drug Facts
69278-110-022022-01-28C16284748780-1d6a99b39-534c-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69278-110-01Cellapy Dr Sanitizer70 mL in 1 TUBEGEL701
69278-110-02Cellapy Dr Sanitizer500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69278-110CELLAPY DR SANITIZER (ALCOHOL) GEL [GM HOLDINGS CO., LTD]1Legacy NDC, 2 package rows20200401_14dde39e-e914-42a6-bf70-8e64d7f29326.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69278-11069278-110-01, 69278-110-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
Propylene Glycol6DC9Q167V3IACT

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
0a6a144a-c341-4a4f-92bb-e08331419af214dde39e-e914-42a6-bf70-8e64d7f293262020-03-20WarningsExact identifier
spl id: 0a6a144a-c341-4a4f-92bb-e08331419af2
spl set id: 14dde39e-e914-42a6-bf70-8e64d7f29326

Reported adverse events (FAERS/openFDA)#

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