FDA.reportPublic FDA data

SAFE SANITIZE ADVANCE HAND SANITIZER

Manufacturer
Eksa Mills, S.A. de C.V.
Effective date
2020-05-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:29:31

Label at a glance#

ProductSAFE SANITIZE ADVANCE HAND SANITIZER
Active ingredientALCOHOL
Label structure7 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol SD408 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria on the skin and kills germs

Warning

WARNINGS SECTION

Keep away from heat, fire or flame

For external use only

Keep away from the eye area, In case of contact, rinse eyes thoroughly with water

Do not apply to sore or broken skin

Stop use

OTC - STOP USE SECTION

if irritation occurs, Consul with physycian before using this product

Keep away from children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a poison control center right away

Do not ingest,

OTC - DO NOT USE SECTION

Do not use if seal is broken

Direction,

DOSAGE & ADMINISTRATION SECTION

place enough product in your palm to thoroughly cover your hands, Rub hands together briskly until dry,

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), isopropyl alcohol, Glycerin, isopropyl myristate, tocopherly acetate, acrylates/C10 30 Alkil acrylatecrosspolymer, aloe barbadensis (aloe vera) leaf juice, theobroma cacao (cocoa) seed butter, cannabissativa (hemp) seed oil, tocopheryl acetate (vitamin E) oil, simmondsia chinensis (jojoba)seed oil, citrus aurantium duicis(orange) peel oil, cymbopogon schoenanthus (lemongrass) oil, mentha piperita (peppermint) leaf extraft, melaleca aiternifoila (tea tree) leaf oil, eucalyptus globulus (eucalyptus) leaf extract, rosmarinus officinalis (rosemary) leaf oil, rosa centifolia (rose) flower oil, pogosternon cabin (patchouli) oil, pelargornium graveolens (geranium) leaf oil

Other information

SPL UNCLASSIFIED SECTION

Store below 110° F (43°C). May discolor certain fabrics or surfaces.

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77538-00077538-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
COCOA BUTTER512OYT1CRRIACT
CANNABIS SATIVA SEED OIL69VJ1LPN1SIACT
.ALPHA.-TOCOPHEROLH4N855PNZ1IACT
JOJOBA OIL724GKU717MIACT
ORANGE OILAKN3KSD11BIACT
CYMBOPOGON SCHOENANTHUS OILXE7K568ILOIACT
MENTHA PIPERITA LEAFA389O33LX6IACT
TEA TREE OILVIF565UC2GIACT
EUCALYPTUS GLOBULUS LEAFS546YLW6E6IACT
ROSEMARY OIL8LGU7VM393IACT
ROSA CENTIFOLIA FLOWER OILH32V31VMWYIACT
POGOSTEMON CABLIN LEAF OILF3IN55X5POIACT
GERANIUM OIL, ALGERIAN TYPE5Q1I94P4WGIACT
ALCOHOL3K9958V90MACTIB

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
dd057dec-96f6-52c8-e053-2a95a90a2b697fed3d2b-44cf-4887-a07d-6dff58a79d2a2022-04-19WarningsExact identifier
spl set id: 7fed3d2b-44cf-4887-a07d-6dff58a79d2a

Reported adverse events (FAERS/openFDA)#

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