FOREST LAB HAND SANITIZER GREEN

Manufacturer
Kosney Inc. | HAPPYCOSMETIC CO.,LTD.
Effective date
2020-07-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:22:14

Label at a glance#

ProductFOREST LAB HAND SANITIZER GREEN
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

• Hand sanitizer to reduce bacteria on the skin that potentially can cause disease

Dosage and administration

• Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry. • No need to wash or rinse hands or use towels • Supervise children in the use of this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 69% w/w

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Carbomer, Aminomethyl Propanol, Glycerin, Camellia Sinensis Leaf Extract, Salvia Officinalis (Sage) Leaf Extract, Centella Asiatica Leaf Extract, Fragrance

PURPOSE

OTC - PURPOSE SECTION

ANTISEPTIC

WARNINGS

WARNINGS SECTION

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 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

• Hand sanitizer to reduce bacteria on the skin that potentially can cause disease

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.
• No need to wash or rinse hands or use towels
• Supervise children in the use of this product.

Other Information

OTHER SAFETY INFORMATION

• Store between 15-30℃ (59-86℉)
• Avoid freezing and excessive heat above 43℃ (110℉)
• May discolor certain fabrics or surfaces

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2287763ethanol 69 % Topical GelPSN1
2287763ethanol 0.69 ML/ML Topical GelSCD1
2287763ethanol 69 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79704-020-022021-07-23C16284748780-1c7ccaba7-1128-fd44-e053-dadaa90aa01b5c6d7fb3-b4ec-47aa-acc6-7d832542932d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79704-020-01FOREST LAB HAND SANITIZER GREEN2 mL in 1 PACKETGEL21
79704-020-02FOREST LAB HAND SANITIZER GREEN20 in 1 CARTONGEL201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79704-020FOREST LAB HAND SANITIZER GREEN (ETHYL ALCOHOL) GEL [KOSNEY INC.]1Legacy NDC, 2 package rows20200723_5c6d7fb3-b4ec-47aa-acc6-7d832542932d.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79704-02079704-020-01, 79704-020-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
b05fe630-8853-460b-93d3-ce28cde5f5e15c6d7fb3-b4ec-47aa-acc6-7d832542932d2020-07-22WarningsExact identifier
spl id: b05fe630-8853-460b-93d3-ce28cde5f5e1
spl set id: 5c6d7fb3-b4ec-47aa-acc6-7d832542932d

Reported adverse events (FAERS/openFDA)#

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