FDA.reportPublic FDA data

ProtectMe Hand Sanitizer Gel

Manufacturer
LNW Protection LLC
Effective date
2020-10-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:11:43

Label at a glance#

ProductProtectMe Antiseptic Hand Sanitizer
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
  • recommended for repeated use

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

  • wet hands thoroughly with product
  • allow to dry without wiping
  • supervise children under 6 years old
  • not recommended for infants

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, Carbomer, Aloe Vera Leaf Extract, Propylene Glycol, Fragrance Aloe Vera, Aminomethyl Propanol, Denatonium Benzoate

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

NDC 80029-009-03

PROTECTME

ANTISEPTIC HAND SANITIZER GEL

with Aloe Vera extract

NON-STICKY

QUICK DRYING

KEEP YOUR HANDS CLEAN

75% ALCOHOL FORMULA

8 FL OZ (250 ml)

80029-009 Rev 10-202080029-009 Rev 10-2020

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
80029-00980029-009-01, 80029-009-07, 80029-009-02, 80029-009-03, 80029-009-06, 80029-009-09, 80029-009-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MACTIB
DENATONIUM BENZOATE4YK5Z54AT2IACT
WATER059QF0KO0RIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAFZY81Z83H0XIACT

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
cfbc2b6d-2889-ae11-e053-2a95a90a1ca1afd8806b-b9ed-ae4e-e053-2995a90aad432021-11-01WarningsExact identifier
spl set id: afd8806b-b9ed-ae4e-e053-2995a90aad43

Reported adverse events (FAERS/openFDA)#

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