Cosforu Safe Hand Sanitizer

Manufacturer
Natuzen Co.,Ltd.
Effective date
2020-04-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:36:49

Label at a glance#

ProductBenoa ACM Hand Sanitiser
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol

INACTIVE INGREDIENT SECTION

Water, carbomer, Triethanolamine, glycerin, propylene glycol, panthenol, dipotassium glycyrrhizate, aloe barbadensis leaf juice, sodium hyaluronate, tocopheryl acetate

OTC - PURPOSE SECTION

instant health care personnel hand antiseptic to reduce bacteria that potentially can cause disease

instant hand antiseptic to decrease bacteria on the skin

WARNINGS SECTION

For external use only when using this product
• If the following abnormal symptoms persist, discontinue use irritation around the eyes, ears,
mucous membranes, including the mouth, irritation or rashes on the skin.
• Stop use immediately and consult a doctor if you experience the following :
1) Hypersensitivity symptoms such as erythema, itching and dermatitis.
2) Skin irritation
3) Follow instructions when using medication.
(1) For external use only (Do not use internally)
(2) Avoid getting into the eyes (If contact occurs, rinse thoroughly with clean water)
• Be careful not to inhale or use for extended periods of time (inhalation of ethanol
repeatedly can cause irritation to mucous membranes and headaches or other symptoms
may appear. When used repeatedly on the same area, skin irritation may occur.
• Do not use the product on the same areas for extended periods of time as swelling,
inflammation or sickness may occur due to absorption through the skin.
It is not recommended to use on areas with open wounds that have been medically treated
with a cast or bandage.
• Do not use in combination with soap or antibacterial cleansing agents.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• Keep Out of Reach of Children.

INDICATIONS & USAGE SECTION

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

DOSAGE & ADMINISTRATION SECTION

for topical use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70930-20270930-202-01, 70930-202-02, 70930-202-03

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
8aa9d1c8-3a8b-4900-8498-5937fad97fa1a273e461-20e0-44f2-e053-2a95a90aa9c62022-11-17WarningsExact identifier
spl set id: a273e461-20e0-44f2-e053-2a95a90aa9c6

Reported adverse events (FAERS/openFDA)#

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