Sani-Professional Sani-Hands

Manufacturer
Professional Disposables International Inc.
Effective date
2021-10-15
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:32:19

Label at a glance#

ProductSani-Professional Sani-Hands made with Tencel
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizer to decrease bacteria on the skin. Dries in seconds.

Dosage and administration

Open packet. USe entire wpe to thoroughly wipe hands, fingers and wrists.To sanitize, useuse multiple wipes. Discard after single use.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

65.9% alcohol by volume

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to decrease bacteria on the skin. Dries in seconds.

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame. For external use only. Do not use in or contact the eyes. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a physician.

Keep this out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Centerright away

Directions

DOSAGE & ADMINISTRATION SECTION

Open packet. USe entire wpe to thoroughly wipe hands, fingers and wrists.To sanitize, useuse multiple wipes. Discard after single use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin, Aloe Barbedensis Leaf juice, Tocopheryl Acetate

Principal Display Panel - 1 ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sani Professional Brand
Sani-Hands

Hand Instant Sanitizing Wipes

  • Kills 99.99% of germs
  • Cleans more effectively than gels
  • FDA Food Code Compliant

1 wipes individually wrapped

6.0 x 5.0 in (15.2 x 12.7 cm)

Packet: packetpacket

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
10819-392210819-3922-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
ce6b4719-d630-0d96-e053-2a95a90a50a424ae1483-6c71-7435-e054-00144ff8d46c2021-10-15WarningsExact identifier
spl id: ce6b4719-d630-0d96-e053-2a95a90a50a4
spl set id: 24ae1483-6c71-7435-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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