LACTONE HAND SANITIZER WIPE

Manufacturer: ALL ONE KOZMETIK SANAYI DIS TICARET ANONIM SIRKETI | HARDAL GLOBAL CONSULTING LLC.
Effective date: 2020-06-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:18:25

Label at a glance#

ProductLACTONE HAND SANITIZER WIPE

Active ingredientALCOHOL

Label structure10 sections

Dosage and administration

wet hands thorougly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 80%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

Use for hand-washing to decrease bacteria on the skin, only when water is not available

Warnings

WARNINGS SECTION

Flammable, keep away from heat and flames. For external use only

OTC - WHEN USING SECTION

When using this product

do not get into eyes

if contact occurs, rinse eyes thoroughly 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

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 thorougly with product and allow to dry without wiping

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, Aloe Barbadensis Leaf Extract and propylene glycol

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Producer

ALL ONE KOZMETIK SAN. VE DIS. TIC. A. S.

Sutluce Mahallesi

Uzunbayır Sokak No:44/4

Beyoglu/Istanbul

Net weight: 5 gr

MADE IN TURKEY

Hand Sanitizer Wipe

Kills 99.99% of E. coli, Salmonella enterica and Staphylococcus aureus (MRSA)

with ALOE VERA FRAGRANCE

For External Use only

LACTONE HAND SANITIZING WIPES- alcohol cloth

puch

Package

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2361646	ethanol 80 % Medicated Pad	PSN	1
2361646	ethanol 0.8 ML/ML Medicated Pad	SCD	1
2361646	ethanol 80 % Medicated Wipes	SY	1
2361646	ethyl alcohol 80 % Topical Cloth	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75348-888-05	2021-07-23	C162847	48780-1	c7ccaba7-10c2-fd44-e053-dadaa90aa01b	Hand Sanitizer Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75348-888-05	LACTONE HAND SANITIZER WIPE	5 g in 1 POUCH	CLOTH	5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75348-888	LACTONE HAND SANITIZER WIPE (ALCOHOL) CLOTH [ALL ONE KOZMETIK SANAYI DIS TICARET ANONIM SIRKETI]	1	Legacy NDC, 1 package rows	20200620_a85e92a2-5702-5957-e053-2a95a90a6a9e.zip

Products#

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

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

LACTONE HAND SANITIZER WIPE
ALCOHOL
ALOE VERA LEAF
PROPYLENE GLYCOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75348-888	75348-888-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALOE VERA LEAF	ZY81Z83H0X	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
a85e8bd8-bee6-8957-e053-2995a90a914f			a85e92a2-5702-5957-e053-2a95a90a6a9e	2020-06-18	Warnings	Exact identifier spl id: a85e8bd8-bee6-8957-e053-2995a90a914f spl set id: a85e92a2-5702-5957-e053-2a95a90a6a9e

Reported adverse events (FAERS/openFDA)#

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