FDA.reportPublic FDA data

Advanced Alcohol Foaming Hand Sanitizer

Manufacturer
Betco Corporation, Ltd.
Effective date
2019-08-01
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-02 00:17:21

Label at a glance#

ProductAdvanced Alcohol Foaming Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Uses Use 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

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

Warnings

WARNINGS SECTION

Warnings

  • For external use only. Do not ingest.
  • FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition.
  • Avoid contact with eyes. In case of eye contact, flush with large quantities of water, seek medical attention if irritation persists.
  • If skin irritation develops, discontinue use. If irritation persists for more than 72 hours, seek medical attention.
  • 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, PEG-10 Dimethicone, PEG-10 Acrylate/Perfluorohexylethyl Acrylate

Copolymer, Perfluorohexylethyl Alcohol, Propylene Glycol, Fragrance, D&C

Green #5.

Purpose

OTC - PURPOSE SECTION

Purpose

Antiseptic

Advanced Alcohol Foaming Hand Sanitizer

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Advanced Alcohol Foaming Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79504-0079504-00

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65601-79565601-795-04, 65601-795-53, 65601-795-57, 65601-795-29, 65601-795-03, 65601-795-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
2-(PERFLUOROHEXYL)ETHANOLG2R5YO5N3VIACT
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PEG-10 ACRYLATEF4663X97LWIACT
D&C GREEN NO. 58J6RDU8L9XIACT
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
ALCOHOL3K9958V90MACTIB

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
aa936369-a4c3-8ecf-e053-2a95a90a43238ee5c43a-592e-4af9-e053-2a95a90abc9e2020-07-16WarningsExact identifier
spl set id: 8ee5c43a-592e-4af9-e053-2a95a90abc9e

Reported adverse events (FAERS/openFDA)#

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