Hand Sanitizer Gel

Manufacturer
Zep Inc.
Effective date
2025-12-26
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:28:49

Label at a glance#

ProductHand Sanitizer Gel
Active ingredientALCOHOL
Label structure13 sections

Indications and uses

■ To help reduce bacteria that can potentially cause disease ■ For use when soap and water are not available

Dosage and administration

■ For occasional and personal use. ■ Rub thoroughly into hands for at least 30 seconds. Allow to dry. ■ Children under 6 years should be supervised when using this product.

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 bacteria that can potentially cause disease

■ For use when soap and water are not available

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from source of heat or fire

Do Not Use

OTC - DO NOT USE SECTION

■ on children less than 2 months of age

■ on open skin wounds

■ on broken or damaged skin

When using this product

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not inhale.

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and lasts.

Keep out of reach of children and pets

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets. In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

■ For occasional and personal use.

■ Rub thoroughly into hands for at least 30 seconds. Allow to dry.

■ Children under 6 years should be supervised when using this product.

Other information

OTHER SAFETY INFORMATION

■ store at a temperature below 110 °F (43 °C).

■ may discolor certain fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Triisopropanolamine, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tocopheryl Acetate.

Questions?

OTC - QUESTIONS SECTION

1-800-514-6729

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

137-4508137-4508

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN6
581662ethanol 0.7 ML/ML Topical GelSCD6
581662ethanol 70 % Topical GelSY6
581662ethyl alcohol 70 % Topical GelSY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66949-137-08Hand Sanitizer Gel2840 mL in 1 CASELIQUID28406
66949-137-28Hand Sanitizer Gel15140 mL in 1 CASELIQUID151406

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
66949-13766949-137-28, 66949-137-08

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
Hand Sanitizer GelETHANOLZep Inc.c72cf71f-e639-2854-e053-2a95a90ab30e2025-12-26WarningsExact identifier
ndc (package): 66949-137-28
ndc (package): 66949-137-08
ndc (product): 66949-137
ndc11 (package): 66949013708
ndc11 (package): 66949013728
spl id: 46deb1c0-3613-1a6b-e063-6394a90a30f9
spl set id: c72cf71f-e639-2854-e053-2a95a90ab30e

Reported adverse events (FAERS/openFDA)#

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