FDA.reportPublic FDA data

Sani-Hands Bedside Pack NDC 10819-3918-1

Manufacturer
Professional Disposables International Inc
Effective date
2026-10-19
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
daily-update
Hydrated at
2026-10-22 02:01:58

Label at a glance#

ProductPDI Sani Hands
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

To decrease bacteria on the skin

Dosage and administration

Peel back label slowly. Pull out wipe and reseal label. Thoroughly wipe hands, fingers, and wrists using entire wipe Allow to dry For dirty hands, use first wipe to clean hands, then discard wipe; sanitize with second wipe. Discard after single use.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% by volume

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • To decrease bacteria on the skin

Warnings

WARNINGS SECTION

  • For external use only
  • Flammable. Keep away from fire or flame.
  • When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
  • Discontinue use if irritation and redness develop. If conditions persist for more than 72 hours, consult a doctor.

Keep this out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children unless under adult supervision.

If swallowed, get medical help or contact a Poison Control Center immediately

Directions

DOSAGE & ADMINISTRATION SECTION

  • Peel back label slowly.
  • Pull out wipe and reseal label.
  • Thoroughly wipe hands, fingers, and wrists using entire wipe
  • Allow to dry
  • For dirty hands, use first wipe to clean hands, then discard wipe; sanitize with second wipe.
  • Discard after single use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

aloe barbadensis leaf juice, glycerin, propylene glycol, purified water, tocopheryl acetate

Principal Display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Web:

WebWeb

Reseal:

ResealReseal

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeCode 128(01)00310819001083GTIN-14: 00310819001083
GTIN-12: 310819001083
UPC-A: 310819001083
EAN-13: 0310819001083
GTIN storage (14 digits): 00310819001083		2HP715.jpg
Data codeData Matrix2HP7152HP715.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10819-3918-12020-10-14C16284748780-1ab0e2407-268a-f274-e053-dbdaa90a6471Sani-Hands Bedside Pack NDC 10819-3918-1
10819-3918-12020-10-14C16284748780-1ab0e2407-268a-f274-e053-dbdaa90a6471Sani-Hands Bedside Pack NDC 10819-3918-1
10819-3918-12020-09-27C16284748780-1ab0e2407-268a-f274-e053-dbdaa90a6471Sani-Hands Bedside Pack NDC 10819-3918-1
10819-3918-12020-09-27C16284748780-1ab0e2407-268a-f274-e053-dbdaa90a6471Sani-Hands Bedside Pack NDC 10819-3918-1
10819-3918-12020-09-25C16284748780-1ab0e2407-268a-f274-e053-dbdaa90a6471Sani-Hands Bedside Pack NDC 10819-3918-1
10819-3918-12020-09-25C16284748780-1ab0e2407-268a-f274-e053-dbdaa90a6471Sani-Hands Bedside Pack NDC 10819-3918-1
10819-3918-12020-07-22C16284748780-1ab0e2407-268a-f274-e053-dbdaa90a6471Sani-Hands Bedside Pack NDC 10819-3918-1
10819-3918-12020-07-22C16284748780-1ab0e2407-268a-f274-e053-dbdaa90a6471Sani-Hands Bedside Pack NDC 10819-3918-1

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
10819-391810819-3918-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALOE BARBADENSIS LEAFZY81Z83H0XIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERINPDC6A3C0OXIACT

Source Document#

Source XML · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82025-07-01full-release2026-06-01 01:06:11

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
38e2ccee-229c-6766-e063-6394a90abfa42fff2a3d-5ea9-346e-e054-00144ff8d46c2025-07-01WarningsExact identifier
spl set id: 2fff2a3d-5ea9-346e-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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