FDA.reportPublic FDA data

Zep E-2 Foaming Sanitizing Hand Cleaner

Manufacturer
Zep Inc.
Effective date
2021-11-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:27:44

Label at a glance#

ProductZep E-2 Foaming Sanitizing Hand Cleaner
Active ingredientCHLOROXYLENOL
Label structure12 sections

Indications and uses

Hand sanitizing to decrease bacteria on the skin.

Dosage and administration

We hands with water. Apply liquid Soap. Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles. Rinse hands thoroughly and dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 3.0%

Purpose

OTC - PURPOSE SECTION

Antiseptic Hand Wash

Uses

INDICATIONS & USAGE SECTION

Hand sanitizing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only. Do not usein or around the eyes; if in eyes, rinse promptly and thoroughly with water.

When using this product

OTC - WHEN USING SECTION

  • Avoid eye contact.
  • If in the eyes, rinse promptly and throoughly with water. Do not swallow.
  • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to dring and consult a physician immediately.
  • Allergy Alert: May cause skin reactions. Symptoms may include: skin reddening, blisters and rash. If a skin reaction occurs, stop use and seek medical help right away.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.

Keep out of reach of children and pets

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets. Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • We hands with water.
  • Apply liquid Soap.
  • Massage soap into hands and wrists, emphasizing back of hands, knuckles and cuticles.
  • Rinse hands thoroughly and dry.

Other information

OTHER SAFETY INFORMATION

  • Store at 20 to 25°C (68 to 77°F).
  • Dispose in accordance with all applicable federal, local and state regulations.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodium C14-16 Olefin Sulfonate, Triethylene Glycol, Cocamidopropyl Betain, Sodium Xylenesulfonate, PEG-75 Lanolin, Citric Acid

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-800-I-BUY-ZEP (1-800-428-9937)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

115_0994115_0994

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66949-11566949-115-16, 66949-115-24

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
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
TRIETHYLENE GLYCOL3P5SU53360IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM XYLENESULFONATEG4LZF950URIACT
PEG-75 LANOLIN09179OX7TBIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
CHLOROXYLENOL0F32U78V2QACTIB

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
f1ed7811-cdce-23f4-e053-2a95a90af36bb43d1b61-3f09-4cb0-e053-2995a90a44092023-01-10WarningsExact identifier
spl set id: b43d1b61-3f09-4cb0-e053-2995a90a4409

Reported adverse events (FAERS/openFDA)#

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