FDA.reportPublic FDA data

Zep Non Alcohol Foam Sanitizer

Manufacturer
Zep Inc.
Effective date
2023-10-20
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 21:23:45

Label at a glance#

ProductZep Non Alcohol Foam Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure12 sections

Indications and uses

Kills 99.99% of most common germs that cause illness in as little as 15 seconds. Sanitizing to decrease bacteria on skin. No rinsing required. Does not contain alcohol.

Dosage and administration

Press pump to dispense product onto hands. Rub hands together allowing foam to contact all areas, especially around the nails. Continue until foam has disappeared and/or hands are dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic Hand Wash

Uses

INDICATIONS & USAGE SECTION

  • Kills 99.99% of most common germs that cause illness in as little as 15 seconds.
  • Sanitizing to decrease bacteria on skin.
  • No rinsing required.
  • Does not contain alcohol.

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

  • Do not swallow.
  • If swallowed, do not induce vomiting and if individual is conscious, give large quantities of water to drink and consult a physician immediately.

Stop using 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

  • Press pump to dispense product onto hands.
  • Rub hands together allowing foam to contact all areas, especially around the nails.
  • Continue until foam has disappeared and/or hands are dry.

Other information

OTHER SAFETY INFORMATION

  • Store at 20 to 25°C (68 to 77°F).
  • Do not freeze.
  • Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, PEG/PPG-18/18 Dimethicone, DMDM Hydantoin and Iodopropynyl Butylcarbamate, Hydroxypropyl Methylcellulose

Questions or comments?

OTC - QUESTIONS SECTION

Call 1-877-I-BUY-ZEP (1-877-428-9937)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

107_1248107_1248

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
66949-10766949-107-16

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT
PEG/PPG-18/18 DIMETHICONE9H0AO7T794IACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
HYPROMELLOSE, UNSPECIFIED3NXW29V3WOIACT
WATER059QF0KO0RIACT
DMDM HYDANTOINBYR0546TOWIACT

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
07ea6980-5fe3-1ca3-e063-6394a90ade5ea63be465-fcef-63ff-e053-2995a90a87c72023-10-20WarningsExact identifier
spl id: 07ea6980-5fe3-1ca3-e063-6394a90ade5e
spl set id: a63be465-fcef-63ff-e053-2995a90a87c7

Reported adverse events (FAERS/openFDA)#

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