FDA.reportPublic FDA data

Personal Sanitizing Wipes

Manufacturer
Sanitizer Supply, LLC
Effective date
2020-11-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:08:18

Label at a glance#

ProductPersonal Sanitizing Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Storage and handling

Other information store between 15-30C (59-86F) avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                                                              Purpose

Benzalkonium Chloride 0.13%...........................................Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • For handwashing to decrease bacteria on skin after assisting ill persons or before contact with a person under medical care or treatment recommended for repeated use

OTC - PURPOSE SECTION

Purpose

Antiseptic

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product

  • keep out of eyes.  In case of contact with eyes, flush thoroughly with water.
  • avoid contact with broken skin
  • do not inhale or ingest

OTC - STOP USE SECTION

Stop use and ask a doctor

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or ocntact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • wet hands thoroughly with product and allow to dry
  • for children under 6, use only under adult supervision
  • not recommended for infants

STORAGE AND HANDLING SECTION

Other information

  • store between 15-30C (59-86F)
  • avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENT SECTION

Inactive Ingredients

purified water USP, fragrance

SPL UNCLASSIFIED SECTION

Questions?

770-875-8967

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90026-11190026-111-90

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
LIMONENE, (+)-GFD7C86Q1WIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
ddb9c67d-2033-5fa4-e053-2995a90a840c32c49a1c-ec3d-406b-bf69-8341333912872022-04-28WarningsExact identifier
spl set id: 32c49a1c-ec3d-406b-bf69-834133391287

Reported adverse events (FAERS/openFDA)#

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