FDA.reportPublic FDA data

Germ Free Sanitizing

Manufacturer
ESC Brands, LLC
Effective date
2021-10-07
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:33:46

Label at a glance#

ProductGerm Free Sanitizing
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

Handwash to help reduce bacteria that potentially can cause disease Helps to prevent cross- contamination by hand contact Helps to prevent drying of skin Recommended for repeat use

Dosage and administration

Wet Hands and wrists with clean running water Apply appropriate amount of product Lather and scrub hands, fingers, fingernails, cuticles and wrists thoroughly Rinse thoroughly with running water Dry hands completely (incomplete drying may result in chapped skin)

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose:

OTC - PURPOSE SECTION

Antiseptic Hand Soap

Uses:

INDICATIONS & USAGE SECTION

  • Handwash to help reduce bacteria that potentially can cause disease
  • Helps to prevent cross- contamination by hand contact
  • Helps to prevent drying of skin
  • Recommended for repeat use

Warnings:

WARNINGS SECTION

  • For external use only

When using this product

OTC - WHEN USING SECTION

do not use in or near eyes

Stop use and ask doctor if

OTC - STOP USE SECTION

irritation and redness develop

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed. seek medical attention or contact a Posion Control Center immediately.

Directions:

DOSAGE & ADMINISTRATION SECTION

  • Wet Hands and wrists with clean running water
  • Apply appropriate amount of product
  • Lather and scrub hands, fingers, fingernails, cuticles and wrists thoroughly
  • Rinse thoroughly with running water
  • Dry hands completely (incomplete drying may result in chapped skin)

Other Information

SPL UNCLASSIFIED SECTION

Store in a cool dry place below 104° F (40°C)

Inactive Ingredinets:

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice, Aqua, Benzyl Alcohol, Citric Acid, Glycerin, Hydrolysed Silk, Lauramidopropyl Betaine, Phenoxyethanol.

Questions?

OTC - QUESTIONS SECTION

+1(888) 331-8332, Mon-Fri 9:00AM-5:00PM (EST)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabelLabel 2Label 2

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71884-00771884-007-08

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
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
BENZYL ALCOHOLLKG8494WBHIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
GLYCERINPDC6A3C0OXIACT
LAURAMIDOPROPYL BETAINE23D6XVI233IACT
PHENOXYETHANOLHIE492ZZ3TIACT
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
cdc53d01-7378-dd7c-e053-2a95a90a0288379d49d3-ea4f-40c6-a562-d109d7fd26022021-10-07WarningsExact identifier
spl id: cdc53d01-7378-dd7c-e053-2a95a90a0288
spl set id: 379d49d3-ea4f-40c6-a562-d109d7fd2602

Reported adverse events (FAERS/openFDA)#

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