Zep Foaming Hand Sanitizer

Manufacturer
Zep Inc.
Effective date
2021-11-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:27:45

Label at a glance#

ProductZep Foaming Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

To help reduce germs and bacteria on the skin. Recommended for repeated use. No rinsing required.

Dosage and administration

Apply foam to hands. Rub into hands for at least 20 seconds or until dry.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • To help reduce germs and bacteria on the skin.
  • Recommended for repeated use.
  • No rinsing required.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire, flame or spark.

For external use only.
Do not use in the eye; if in eyes, rinse 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 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

  • Apply foam to hands.
  • Rub into hands for at least 20 seconds or until dry.

Other information

OTHER SAFETY INFORMATION

  • Keep container closed and stored in a dry area at temperatures between 68°F to 77°F (20°C and 25°C).
  • Do not reuse empty container.
  • Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Acrylates/Perfluorohexylethyl Methacrylate Copolymer (and) Perfluorohexylethyl Alcohol, Aloe Barbadensis Leaf Juice

Questions or comments?

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

138-3285138-3285

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66949-13866949-138-24, 66949-138-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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-cdcc-23f4-e053-2a95a90af36bc72cf71f-e63a-2854-e053-2a95a90ab30e2023-01-10WarningsExact identifier
spl set id: c72cf71f-e63a-2854-e053-2a95a90ab30e

Reported adverse events (FAERS/openFDA)#

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