FDA.reportPublic FDA data

Sani Pro Sani-Hands Antibacterial Wipe

Manufacturer
Professional Disposables International Inc
Effective date
2023-10-09
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:24:41

Label at a glance#

ProductSani Pro Sani-Hands Antibacterial Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Dosage and administration

To dispense, lift cover, remove seal, pull center sheet from roll, twist to a point, and feed through dispenser hole in cover. Keep cap closed to prevent moisture loss. Use entire wipe to thoroughly wipe hands, fingers and wrists. To sanitize, use multiple wipes. Discard after single use.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%w/w

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

To decrease bacteria on the skin

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable, keep away from fire or flame
  • If swallowed, get medical help or contact a Poison Control Center right away.
  • Do not use in or contact the the eyes.
  • Discontiue use if irritation and redness develp. If condition persists for more than 72 hours, consult a doctor

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this out of reach of children unless under adult supervision

Directions

DOSAGE & ADMINISTRATION SECTION

  • To dispense, lift cover, remove seal, pull center sheet from roll, twist to a point, and feed through dispenser hole in cover. Keep cap closed to prevent moisture loss.
  • Use entire wipe to thoroughly wipe hands, fingers and wrists.
  • To sanitize, use multiple wipes.
  • Discard after single use.

Other information

OTHER SAFETY INFORMATION

Lot No. and Expiration Date can be found on canister.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Disodium EDTA, Fragrance, PPG-2 Hydroxyethyl Cocamide, Purified Water, SD Alcohol 40, Sorbic Acid

Principal display panels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

front 150 ct

front 150 ctfront 150 ct

back 150 ct

back 150 ctback 150 ct

front 300 ct

front 300 ctfront 300 ct

back 300ct

back 300 ctback 300 ct

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10819-701410819-7014-1, 10819-7014-2

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
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
SORBIC ACIDX045WJ989BIACT
ALOE VERA LEAFZY81Z83H0XIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
EDETATE DISODIUM7FLD91C86KIACT
PPG-2 HYDROXYETHYL COCAMIDE34N07GUJ3XIACT
MICROCITRUS AUSTRALIS FRUIT9DNS80T428IACT

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
074a2d40-1410-466f-e063-6294a90a296e366c6362-ef70-4775-e054-00144ff8d46c2023-10-09WarningsExact identifier
spl id: 074a2d40-1410-466f-e063-6294a90a296e
spl set id: 366c6362-ef70-4775-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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