FDA.reportPublic FDA data

66949-136 / 0900 / LHSS Alcohol Sanitizer Spray

Manufacturer
Zep Inc.
Effective date
2023-10-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:23:46

Label at a glance#

ProductZep Alcohol Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

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

Dosage and administration

Apply santizer to hands. Rub into hands for at least 20 seconds or until 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.
Do not use in the eyes; if in eyes, rinse promptly and thoroughly with water.
Flammable. Keep away from fire, flame or spark.

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 santizer to hands.
  • Rub into hands for at least 20 seconds or until 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; Glycerine

Questions or comments?

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

136-0900136-0900

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
66949-13666949-136-28, 66949-136-32

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
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT

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
07eab1ff-e331-d278-e063-6394a90a4999be118e65-7924-ef60-e053-2a95a90a76082023-10-20WarningsExact identifier
spl id: 07eab1ff-e331-d278-e063-6394a90a4999
spl set id: be118e65-7924-ef60-e053-2a95a90a7608

Reported adverse events (FAERS/openFDA)#

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