FDA.reportPublic FDA data

HSUS Antiseptic Hand Sanitizer IPA

Manufacturer
Health Supply Us, LLC | Shotwell Hydrogenics
Effective date
2021-12-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:45:29

Label at a glance#

ProductHSUS Antiseptic Hand Sanitizer IPA
Active ingredientISOPROPYL ALCOHOL
Label structure7 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

Isopropyl 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

Water, Polyethylene glycol, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice, Glycerin, Tocopheryl Acetate

Questions or comments?

OTC - QUESTIONS SECTION

1-888-408-1694

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

10x10 NDC 81342-002-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581698isopropyl alcohol 70 % Topical GelPSN2
581698isopropyl alcohol 0.7 ML/ML Topical GelSCD2
581698isopropyl alcohol 70 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81342-003-012022-07-29C16284748780-1e4f33bdf-b1eb-d8a0-e053-dadaa90a6e4eHSUS Antiseptic Hand Sanitizer IPA

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81342-003-01HSUS Antiseptic Hand Sanitizer IPA1.5 mL in 1 POUCHGEL1.52
81342-003-01HSUS Antiseptic Hand Sanitizer IPA10 in 1 BOXGEL102

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81342-003HSUS ANTISEPTIC HAND SANITIZER IPA (ALCOHOL) GEL [HEALTH SUPPLY US, LLC]2Legacy NDC, 2 package rows20211208_c090753f-a838-1abf-e053-2995a90a6c5f.zip

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
81342-00381342-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACRYLATES/VINYL ISODECANOATE CROSSPOLYMER (10000 MPA.S NEUTRALIZED AT 0.5%)2N8MDB79NAIACT
ALOE VERA LEAFZY81Z83H0XIACT
POLYETHYLENE GLYCOL, UNSPECIFIED3WJQ0SDW1AIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT

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
d2965eab-f160-64a7-e053-2a95a90a82c4c090753f-a838-1abf-e053-2995a90a6c5f2021-12-07WarningsExact identifier
spl id: d2965eab-f160-64a7-e053-2a95a90a82c4
spl set id: c090753f-a838-1abf-e053-2995a90a6c5f

Reported adverse events (FAERS/openFDA)#

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