SANOTIS HAND CLEANER

Manufacturer
MEGACOS MANUFACTURING Co., Ltd.
Effective date
2020-05-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:28:28

Label at a glance#

ProductSANOTIS HAND CLEANER
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

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

Dosage and administration

• Place enough product on hands to cover all surface. Rub hands together until dry. • Supervise children under 6 years of age when using this product to avoid swallowing. • Avoid direct inhalation of vapors during application. (Headaches and irritation to mucous membranes may occur when directly inhaled.) • This product is intended only for sanitizing. • To prevent contents from drying out and contaminants from en...

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Alcohol 65%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

water, glycerin, caprylyl glycol, allantoin, artemisia princeps leaf extract, butylene glycol, dipotassium glycyrrhizate, ethylhexylglycerin, mentha piperita (peppermint) oil, 1,2-hexandiol, sodium hyaluronate

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 eyes thoroughly with water.
----------------------------------------------------------------------- ---------------------------------
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

Uses

INDICATIONS & USAGE SECTION

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

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.

Directions

DOSAGE & ADMINISTRATION SECTION

• Place enough product on hands to cover all surface. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.
• Avoid direct inhalation of vapors during application. (Headaches and irritation to mucous membranes may occur when directly inhaled.)
• This product is intended only for sanitizing.
• To prevent contents from drying out and contaminants from entering, close lid completely after use.
• Keep product in its original container as storing the product in anything other than the original container may result in accidents or cause the integrity of the product to diminish.
• Do not use over bandage, castings, etc. as irritation occur.

Other information

OTHER SAFETY INFORMATION

• Store between 1-30℃ (33.8-86℉)
• Avoid freezing and excessive heat above 40℃ (104℉)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78063-00178063-001-01, 78063-001-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
2a26d05b-340c-47c4-8c4b-d699f834968ca6c7009e-1b5d-e060-e053-2995a90a07792023-12-05WarningsExact identifier
spl set id: a6c7009e-1b5d-e060-e053-2995a90a0779

Reported adverse events (FAERS/openFDA)#

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