FDA.reportPublic FDA data

Zep Hand Sanitizer

Manufacturer
Zep Inc.
Effective date
2022-12-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:42:26

Label at a glance#

ProductZep Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

Hand sanitizing to decrease bacteria on skin. No rinsing required.

Dosage and administration

Apply sanitizer spray. Rub the spray over hands and let dry. No rinsing or toweling is required.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • Hand sanitizing to decrease bacteria on skin.
  • No rinsing required.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from fire, flame or spark.

When using this product

OTC - WHEN USING SECTION

  • Avoid eye contact.
  • If in eyes, rinse promptly and thoroughly with water.

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.

OTC - ASK DOCTOR SECTION

If swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply sanitizer spray.
  • Rub the spray over hands and let dry.
  • No rinsing or toweling is required.

Other information

OTHER SAFETY INFORMATION

  • Store at 4 to 27°C (40 to 80°F).
  • Dispose in accordance with all applicable federal, state and local regulations.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Deionized Water, Glycerin

Questions or comments?

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

134_R462134_R462

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66949-13466949-134-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT

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
f033be84-553f-36f2-e053-2a95a90a4d32b932c99e-697e-0955-e053-2995a90a853d2022-12-19WarningsExact identifier
spl id: f033be84-553f-36f2-e053-2a95a90a4d32
spl set id: b932c99e-697e-0955-e053-2995a90a853d

Reported adverse events (FAERS/openFDA)#

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