Gio Solution Sanitizer

Manufacturer
GREEN WONIL CO., LTD.
Effective date
2020-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:43

Label at a glance#

ProductGio Solution Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease • instant hand antiseptic to decrease bacteria on the skin

Dosage and administration

Pour a small amount into hands, spread evenly and rub into the skin

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ethanol (Synthetic Alcohol) 70%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Chamomilla Recutita (Matricaria) Extract, Eucalyptus Globulus Leaf Extract, Aminomethyl Propanol

PURPOSE

OTC - PURPOSE SECTION

Disinfecting Agent

WARNINGS

WARNINGS SECTION

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


When using this product
if following abnormal symptoms persist, discontinue use. lrritation 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 lrritation 3) Following instructions when using medication (1) For external use only (Do not use internally) (2) Avoid getting into the eyes (if contact occurs, wash well with clean water)
Be careful not to 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 or sickness may occur 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.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Uses

INDICATIONS & USAGE SECTION

• instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease
• instant hand antiseptic to decrease bacteria on the skin

Directions

DOSAGE & ADMINISTRATION SECTION

Pour a small amount into hands, spread evenly and rub into the skin

Other Information

OTHER SAFETY INFORMATION

- read the directions and warnings before use
- avoid freezing and excessive heat above 40 degree C (104 degree F)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
76532-040-012022-07-29C16284748780-1e4f33bdf-af60-d8a0-e053-dadaa90a6e4e94ba8ef1-62b3-4215-a3f4-e7f52bf06f62

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76532-040-01Gio Solution Sanitizer60 mL in 1 CARTONGEL601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
76532-040GIO SOLUTION SANITIZER (ETHANOL SYNTHETIC ALCOHOL) GEL [GREEN WONIL CO., LTD.]1Legacy NDC, 1 package rows20200603_94ba8ef1-62b3-4215-a3f4-e7f52bf06f62.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76532-04076532-040-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
702126d1-400d-4c21-ac36-db62ae8a442994ba8ef1-62b3-4215-a3f4-e7f52bf06f622020-06-02WarningsExact identifier
spl id: 702126d1-400d-4c21-ac36-db62ae8a4429
spl set id: 94ba8ef1-62b3-4215-a3f4-e7f52bf06f62

Reported adverse events (FAERS/openFDA)#

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