SHABOINK

Manufacturer: Zhejiang Guoyao Jingyue Aerosol Co., Ltd.
Effective date: 2026-01-05
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:31:32

Label at a glance#

ProductSHABOINK

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

hand snitizer to help decrease bacteria on skin. when water soap & towel are not available. recommended for repeated use

Dosage and administration

pump as needed into your palms and thoroughly spread on both hands rub into skin until dry

Storage and handling

store at 20C(68 to 77F) may discolor fabrics.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Warnings

WARNINGS SECTION

For external use only.

Please do not use product if allergic to any ingredients listed.

Flammable. Keep away from fire or flame.

Do not apply around eyes.

Do not use

OTC - DO NOT USE SECTION

Do not use in ears & mouth

When using this product

OTC - WHEN USING SECTION

When using this product, avoid contact with eyes. In case of contact flush eyes with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

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

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product. If swallowed, get medical help or contact a Posion Control Center right away.

Uses

INDICATIONS & USAGE SECTION

hand snitizer to help decrease bacteria on skin.
when water soap & towel are not available.
recommended for repeated use

Directions

DOSAGE & ADMINISTRATION SECTION

pump as needed into your palms and thoroughly spread on both hands
rub into skin until dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

Other information

STORAGE AND HANDLING SECTION

store at 20C(68 to 77F)
may discolor fabrics.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2286295	ethanol 75 % Topical Spray	PSN	2
2286295	ethanol 0.75 ML/ML Topical Spray	SCD	2
2286295	ethanol 75 % Topical Spray	SY	2

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0850009031457	GTIN-13: 0850009031457 EAN-13: 0850009031457 GTIN-12: 850009031457 UPC-A: 850009031457 GTIN storage (14 digits): 00850009031457	label.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75742-005-01	2026-01-05	C162847	48780-1	1030e364-fc3e-111a-e063-dadaa90a10e2	a8c0c9ce-05ac-0f33-e053-2a95a90ab8ed
75742-005-01	2024-01-30	C162847	48780-1	1030e364-fc3e-111a-e063-dadaa90a10e2	a8c0c9ce-05ac-0f33-e053-2a95a90ab8ed

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75742-005-01	SHABOINK	60 mL in 1 BOTTLE, SPRAY	SPRAY	60		2

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

SHABOINK
Ethyl Alcohol
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75742-005	75742-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
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
SHABOINK	ETHYL ALCOHOL	Zhejiang Guoyao Jingyue Aerosol Co., Ltd.	a8c0c9ce-05ac-0f33-e053-2a95a90ab8ed	2026-01-05	Warnings	Exact identifier ndc (package): 75742-005-01 ndc (product): 75742-005 ndc11 (package): 75742000501 spl id: 47afa042-e18c-be26-e063-6394a90a097c spl set id: a8c0c9ce-05ac-0f33-e053-2a95a90ab8ed

Reported adverse events (FAERS/openFDA)#

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