ZEPOL

Manufacturer: DILE ENTERPRISES LLC | DILE ENTERPRISE LLC
Effective date: 2020-06-22
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:18:47

Label at a glance#

ProductZEPOL

Active ingredientALCOHOL

Label structure12 sections

Storage and handling

Store between 15-30C (59-89F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65% v/v. Purpose: Antiseptic

OTC - PURPOSE SECTION

Antisptic, Hand Sanitizer

WARNINGS SECTION

Flammable. Keep awy from fire or flame. For external use.

OTC - DO NOT USE SECTION

In children less than 2 months of age

On open skin wounds

OTC - WHEN USING SECTION

Do not use in eyes. In case of contact with eyes, rinse with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help promptly.

DOSAGE & ADMINISTRATION SECTION

Place enough product on hands to cover all surface. Rub hands together until dry.

Supervise children under 6 years of age when using this product to avoid swallowing

STORAGE AND HANDLING SECTION

Store between 15-30C (59-89F)

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria for the skin.

INACTIVE INGREDIENT SECTION

Water, carbomer, isopropyl alcohol, triethanolamine

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3.785 L Label3.785L NDC 79198-656-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
902574	ethanol 65 % Topical Gel	PSN	1
902574	ethanol 0.65 ML/ML Topical Gel	SCD	1
902574	ethyl alcohol 65 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
79198-656-01	2022-01-28	C162847	48780-1	d6a99b39-f70a-a426-e053-dadaa90af4c2	a8b5223e-2955-5155-e053-2995a90a1f72

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
79198-656-01	ZEPOL	3785 mL in 1 JUG	GEL	3785		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
79198-656	ZEPOL (ETHYL ALCOHOL) GEL [DILE ENTERPRISES LLC]	1	Legacy NDC, 1 package rows	20200624_a8b5223e-2955-5155-e053-2995a90a1f72.zip

Products#

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

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

ZEPOL
Ethyl Alcohol
FENOPROP TRIETHANOLAMINE
ALCOHOL
WATER
ISOPROPYL ALCOHOL
CARBOMER 940

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
79198-656	79198-656-01

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
FENOPROP TRIETHANOLAMINE	2F3CU8K84U	IACT
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT
CARBOMER 940	4Q93RCW27E	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a8b5223e-2956-5155-e053-2995a90a1f72			a8b5223e-2955-5155-e053-2995a90a1f72	2020-06-22	Warnings	Exact identifier spl id: a8b5223e-2956-5155-e053-2995a90a1f72 spl set id: a8b5223e-2955-5155-e053-2995a90a1f72

Reported adverse events (FAERS/openFDA)#

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