Dermokil

Manufacturer: Halshe, LLC | EZEL KOZMETIK ITH. VE IHR. TIC. VE SAN. A.Ş.
Effective date: 2020-04-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:08:21

Label at a glance#

ProductDermokil

Active ingredientALCOHOL

Label structure12 sections

Dosage and administration

- wet hands thoroughly with product - allow to dry without wiping

Storage and handling

Other information - keep out of direct sunlight - store in dry conditions

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 71.5% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged, inflamed or broken skin

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes

In case of eye contact, rinse eyes thoroughly with water

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develops and lasts for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

- wet hands thoroughly with product

- allow to dry without wiping

Other information

STORAGE AND HANDLING SECTION

Other information

- keep out of direct sunlight

- store in dry conditions

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, isopropyl alcohol, sodium hydroxide, purified water USP

Use

INDICATIONS & USAGE SECTION

Use for hand sanitizing to decrease bacteria on the skin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500 ml NDC: 75004-786-55 PDP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2360897	ethanol 71.5 % Topical Gel	PSN	1
2360897	ethanol 0.715 ML/ML Topical Gel	SCD	1
2360897	ethanol 71.5 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75004-786-55	2021-07-23	C162847	48780-1	c7ccaba7-1ad6-fd44-e053-dadaa90aa01b	a44cec41-bb90-811f-e053-2a95a90a1885

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75004-786-55	Dermokil	500 mL in 1 BOTTLE, PUMP	GEL	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75004-786	DERMOKIL (HAND SANITIZER GEL) GEL [HALSHE, LLC]	1	Legacy NDC, 1 package rows	20200428_a44cec41-bb90-811f-e053-2a95a90a1885.zip

Products#

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

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

Dermokil
Hand Sanitizer Gel
SODIUM HYDROXIDE
ALCOHOL
ISOPROPYL ALCOHOL
GLYCERIN
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75004-786	75004-786-55

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
SODIUM HYDROXIDE	55X04QC32I	IACT
ALCOHOL	3K9958V90M	ACTIB
ISOPROPYL ALCOHOL	ND2M416302	IACT
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	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
a44ce0d1-d56e-4a9f-e053-2a95a90a19b3			a44cec41-bb90-811f-e053-2a95a90a1885	2020-04-02	Warnings	Exact identifier spl id: a44ce0d1-d56e-4a9f-e053-2a95a90a19b3 spl set id: a44cec41-bb90-811f-e053-2a95a90a1885

Reported adverse events (FAERS/openFDA)#

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