FDA.reportPublic FDA data

ProtectMe Hand Sanitizer Wipes

Manufacturer
LNW Protection LLC
Effective date
2020-09-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:14:33

Label at a glance#

ProductProtectMe Hand Sanitizer Wipes
Active ingredientALCOHOL
Label structure10 sections

Storage and handling

Other information store between 15°-30°C (59°-86°F). do not store above 40ºC (104ºF) may discolor some fabrics

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 75%

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Uses

to decrease bacteria on the skin

WARNINGS SECTION

Warnings

For external use only

Flammable. Keep away from fire or flame

OTC - WHEN USING SECTION

When using this product keep away from eyes. In case of contact, flush eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or persist 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 contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • pull one sheet from cannister
  • rub wipe thoroughly over all surfaces of both hands and allow to dry
  • close lid after each use to keep wipes fresh

STORAGE AND HANDLING SECTION

Other information

  • store between 15°-30°C (59°-86°F).
  • do not store above 40ºC (104ºF)
  • may discolor some fabrics

INACTIVE INGREDIENT SECTION

Inactive ingredients

Water, Propylene Glycol

SPL UNCLASSIFIED SECTION

Distributed by:

LNW PROTECTION LLC

1191 NEWPORT CENTER DR SUITE 103

DEERFIELD BEACH, FL 33442

INFO@PROTECTMESANITIZER.COM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PROTECTME

HAND SANITIZER WIPES

KEEP YOUR HANDS CLEAN!

75% Alcohol Formula

40 WIPES

7.8in x 5.5in (20cm x 14cm)

Faca Pote Wipes 40-ctFaca Pote Wipes 40-ct

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80029-00380029-003-15, 80029-003-30, 80029-003-40, 80029-003-50

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
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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
cfbc2d4f-f496-5be2-e053-2995a90a779eaffc3b66-b8e2-50b6-e053-2995a90ac4fc2021-11-01WarningsExact identifier
spl set id: affc3b66-b8e2-50b6-e053-2995a90ac4fc

Reported adverse events (FAERS/openFDA)#

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