HSUS Antiseptic Hand Sanitizer Ethyl Alcohol

Manufacturer
Health Supply Us, LLC | VSHAPES SRL
Effective date
2021-02-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:49:57

Label at a glance#

ProductHSUS Antiseptic Hand Sanitizer Ethyl Alcohol
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

For hand washing to decrease bacteria on the skin  recommended for repeated use

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on the skin 
  • recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

in the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists for more than 72 hours

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

Wet hands thoroughly with product and allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acrylates/C10-C30 Alkyl Acrylate Crosspolymer, Triethanolamine, Water

Questions or comments?

OTC - QUESTIONS SECTION

1-888-408-1694

Package Labeling:150sachets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SachetSachet150pk150pk

150pk NDC 81342-001-01

Package Labeling: 10 Sachets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10pk10pk

10 Pack NDC 81342-001-004

Package Labeling:125 sachets

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

125pk125pk

125 pack NDC 81342-001-02

Package Labeling: 25 Pack

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

25pk25pk25 Pack NDC 81342-001-003

Products#

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DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81342-00181342-001-01, 81342-001-02, 81342-001-03, 81342-001-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
bd0d42b7-4250-4802-e053-2a95a90aeaa1bc2e1c7e-63a7-bbec-e053-2a95a90af5702021-03-08WarningsExact identifier
spl set id: bc2e1c7e-63a7-bbec-e053-2a95a90af570

Reported adverse events (FAERS/openFDA)#

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