Abutol PARIS ANTISEPTIC HAND SANITIZER GEL ALOE VERA SCENTED

Manufacturer: ATAK FARMA KOZMETIK VE KIMYA SANAYI TICARET ANONIM SIRKETI
Effective date: 2020-06-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:17:53

Label at a glance#

ProductAbutol PARIS ANTISEPTIC HAND SANITIZER

Active ingredientALCOHOL

Label structure9 sections

Indications and uses

• hand sanitizer to decrease bacteria on the skin • recommended for repeated use • for use when soap and water are not available

Dosage and administration

• wet hands thoroughly with product and allow to dry without wiping • supervise children under 6 years of age when using this product to avoid swallowing

Storage and handling

• store between 15-30°C (59-86°F) • avoid freezing and excessive heat above 40°C (104°F) • may discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

• hand sanitizer to decrease bacteria on the skin
• recommended for repeated use
• for use when soap and water are not available

Warnings

WARNINGS SECTION

Flammable, keep away from fire / flame
For external use only

Do not use• in children less than 2 months of age
• on open skin wounds
When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water. • Do not inhale or ingest.

Stop and ask doctor if
• irritation and redness develop
• condition persists for more than 72 hours

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• wet hands thoroughly with product and allow to dry without wiping
• supervise children under 6 years of age when using this product to avoid swallowing

Other information

STORAGE AND HANDLING SECTION

• store between 15-30°C (59-86°F)
• avoid freezing and excessive heat above 40°C (104°F)
• may discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

carbomer, FD&C Blue No.1 , FD&C Yellow No.5, fragrance, glycerin, triethanolamine, water.

SPL UNCLASSIFIED SECTION

Distributed by: Daisy Distribution LLC, Wood Ridge, NJ 07075
Country Of Origin: Turkey

You may also report any serious side effects to
PO Box 328, Wood Ridge, NJ 07075-328

Lot No: 200620
Exp. Date: 06-2023
NDC: 77418-102-10

661799958882

•No Rinsing Required
•Does Not Dry The Skin

ALCOHOL CONTENT 70%

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Packaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
77418-102-10	2022-01-28	C162847	48780-1	d6a99b39-5add-a426-e053-dadaa90af4c2	Abutol PARIS ANTISEPTIC HAND SANITIZER GEL ALOE VERA SCENTED

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77418-102-10	Abutol PARIS ANTISEPTIC HAND SANITIZER	80 mL in 1 TUBE	GEL	80		1
77418-102-10	Abutol PARIS ANTISEPTIC HAND SANITIZER	1 in 1 CARTON	GEL	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77418-102	ABUTOL PARIS ANTISEPTIC HAND SANITIZER (ETHYL ALCOHOL) GEL [ATAK FARMA KOZMETIK VE KIMYA SANAYI TICARET ANONIM SIRKETI]	1	Legacy NDC, 2 package rows	20200617_8adb1e4a-669e-4cff-af22-42eb13ffb2d1.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Abutol PARIS ANTISEPTIC HAND SANITIZER
Ethyl Alcohol
ALCOHOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
FD&C YELLOW NO. 5
FD&C BLUE NO. 1
GLYCERIN
TROLAMINE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77418-102	77418-102-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
FD&C YELLOW NO. 5	I753WB2F1M	IACT
FD&C BLUE NO. 1	H3R47K3TBD	IACT
GLYCERIN	PDC6A3C0OX	IACT
TROLAMINE	9O3K93S3TK	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
9b375d46-f363-46f2-a886-57c2956629be			8adb1e4a-669e-4cff-af22-42eb13ffb2d1	2020-06-02	Warnings	Exact identifier spl id: 9b375d46-f363-46f2-a886-57c2956629be spl set id: 8adb1e4a-669e-4cff-af22-42eb13ffb2d1

Reported adverse events (FAERS/openFDA)#

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