Antiseptique Plus

Manufacturer: Hubot Healthcare LLC
Effective date: 2020-03-18
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:04:08

Label at a glance#

ProductAntiseptique Plus

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

for handwashing to decrease bacteria on the skin

Dosage and administration

Apply product onto hands, spread thoroughly and rub dry

Storage and handling

For additional information, see Safety Data Sheets (SDS) For emergency medical information in USA and Canada, call 1-888-255-3924 For emergency medical information worldwide, call 1-813-248-0573

Contacts and useful links#

PhoneLabel contact1-888-255-3924

PhoneLabel contact1-813-248-0573

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62.5% w/w

Purposes

OTC - PURPOSE SECTION

Antiseptic handwash

Uses

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only
Flammable, keep away from fire or flame, heat, sparks, and sources of static discharge

Do not use

OTC - DO NOT USE SECTION

In eyes

When using this product

OTC - WHEN USING SECTION

If in eyes, rinse promptly and thoroughly with water
Discontinue use if irritation and redness develops

OTC - STOP USE SECTION

Stop use and ask a doctor if skin irritation or redness occurs or persists for more than 72 hours.

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

Apply product onto hands, spread thoroughly and rub dry

Other Information

STORAGE AND HANDLING SECTION

For additional information, see Safety Data Sheets (SDS)
For emergency medical information in USA and Canada, call 1-888-255-3924
For emergency medical information worldwide, call 1-813-248-0573

Inactive Ingredients

INACTIVE INGREDIENT SECTION

water (aqua), ethyl acrylate/ methacrylic acid/ steareth-20 methacrylate copolymer, aminomethylpropanediol, ppg-14 butyl ether, tocopherol acetate, aloe barbadensis leaf juice

Questions?

OTC - QUESTIONS SECTION

Call 1-855-CLEAN-55 (253-2655)

PRINCIPAL DISPLAY PANEL - 473 ML Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTISEPTIQUE⁺
PLUS
gel sanitizer

antiseptic | rinse-free | 62.5% alcohol

FOR HANDS
dye free, fragrance free

16 FL. OZ. (473 ML)

PRINCIPAL DISPLAY PANEL - 473 ML Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1860080	ethanol 62.5 % Topical Gel	PSN	1
1860080	ethanol 0.625 ML/ML Topical Gel	SCD	1
1860080	ethanol 62.5 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72138-470-06	2021-07-23	C162847	48780-1	c7ccaba7-12a8-fd44-e053-dadaa90aa01b	Antiseptique Plus
72138-470-16	2021-07-23	C162847	48780-1	c7ccaba7-12a8-fd44-e053-dadaa90aa01b	Antiseptique Plus
72138-470-32	2021-07-23	C162847	48780-1	c7ccaba7-12a8-fd44-e053-dadaa90aa01b	Antiseptique Plus

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72138-470-06	Antiseptique Plus	177 mL in 1 BOTTLE, PUMP	GEL	177	1
72138-470-16	Antiseptique Plus	473 mL in 1 BOTTLE, PUMP	GEL	473	1
72138-470-32	Antiseptique Plus	946 mL in 1 BOTTLE, PUMP	GEL	946	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72138-470	ANTISEPTIQUE PLUS (ALCOHOL) GEL [HUBOT HEALTHCARE LLC]	1	Legacy NDC, 3 package rows	20200327_6dc7f218-363f-4bf4-ae0a-1155bbdc6f19.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Antiseptique Plus
ALCOHOL
Water
ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER
AMINOMETHYLPROPANOL
PPG-14 BUTYL ETHER
Aloe Vera Leaf
Tocopherol

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72138-470	72138-470-06, 72138-470-16, 72138-470-32

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
Water	059QF0KO0R	IACT
ETHYL ACRYLATE/METHACRYLIC ACID/STEARETH-20 METHACRYLATE COPOLYMER	EPA1872R1N	IACT
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
PPG-14 BUTYL ETHER	R199TJT95T	IACT
Aloe Vera Leaf	ZY81Z83H0X	IACT
Tocopherol	R0ZB2556P8	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
71a4771b-e392-45f2-9ec3-fe427d97f1a8			6dc7f218-363f-4bf4-ae0a-1155bbdc6f19	2020-03-18	Warnings	Exact identifier spl id: 71a4771b-e392-45f2-9ec3-fe427d97f1a8 spl set id: 6dc7f218-363f-4bf4-ae0a-1155bbdc6f19

Reported adverse events (FAERS/openFDA)#

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