FDA.reportPublic FDA data

Advanced Alcohol Gel Sanitizer II

Manufacturer
Betco Corporation, Ltd
Effective date
2020-05-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:30:46

Label at a glance#

ProductAdvanced Alcohol Gel Sanitizer II
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Uses • Hand sanitizer to reduce microorganisms on the skin. • Use this product when soap and water are not available.

Dosage and administration

Directions • Read the entire label before using this product. • Place enough product on your palm to thoroughly cover your hands. • Rub hands together briskly until dry.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Ethyl Alcohol 70%

Uses

INDICATIONS & USAGE SECTION

Uses

• Hand sanitizer to reduce microorganisms on the skin.

• Use this product when soap and water are not available.

Purpose

OTC - PURPOSE SECTION

Purpose

Antiseptic

Warnings

WARNINGS SECTION

Warnings

• For external use only.

• Avoid contact with eyes. If contact occurs, rinse thoroughly with water.

• FLAMMABLE. This product contains ethyl alcohol. Keep away from

sources of ignition.

• Discontinue use if irritation or redness develops.

• If irritation persists for more than 72 hours, consult a physician.

• KEEP OUT OF REACH OF CHILDREN.

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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

• Read the entire label before using this product.

• Place enough product on your palm to thoroughly cover your hands.

• Rub hands together briskly until dry.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients

Water, Diisopropanolamine, PEG-6 (and) AMP- Acrylates/Vinyl Isodecanoate Crosspolymer,
Glycerin, PEG/PPG-8/3 Laurate, Aloe Barbadensis Leaf Juice

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

65601-797-0465601-797-04

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
65601-79765601-797-55, 65601-797-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEG-8 LAURATE762O8IWA10IACT
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
DIISOPROPANOLAMINE0W44HYL8T5IACT
POLYETHYLENE GLYCOL 1000U076Q6Q621IACT
WATER059QF0KO0RIACT
TERT-BUTYL ALCOHOLMD83SFE959IACT
ALOE VERA LEAFZY81Z83H0XIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT

Source Document#

Source XML · Source PDF

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
af0c4eed-dd2d-c559-e053-2a95a90a8152a5a139c4-c180-2e51-e053-2995a90ae5dd2020-09-11WarningsExact identifier
spl set id: a5a139c4-c180-2e51-e053-2995a90ae5dd

Reported adverse events (FAERS/openFDA)#

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