hand sanitizer

Manufacturer: Taizhou Yadai Daily-Use Co., Ltd.
Effective date: 2020-04-14
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:06:17

Label at a glance#

Producthand sanitizer

Active ingredientALCOHOL

Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Keep out of direct sunligh

INACTIVE INGREDIENT SECTION

water

WARNINGS SECTION

FOR EXTERNAL USEONLY. Avoid contatwitheyes. If eye contact occours,fush with water. Keep out of direct sunlight

INDICATIONS & USAGE SECTION

purmp onto hands, lteregrously for atleast 15second, rise and dry throughly

OTC - ACTIVE INGREDIENT SECTION

ethyl alcohol

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of children

OTC - PURPOSE SECTION

Disinfection
Sterilization

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
247835	ethanol 62 % Topical Solution	PSN	2
247835	ethanol 0.62 ML/ML Topical Solution	SCD	2
247835	ethanol 62 % Topical Solution	SY	2
247835	ethyl alcohol 62 % Topical Solution	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
52989-001-01	2021-07-23	C162847	48780-1	c7ccaba7-0fbd-fd44-e053-dadaa90aa01b	a2c2df88-ebed-dfe4-e053-2995a90ae08b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
52989-001-01	hand sanitizer	60 mL in 1 BOTTLE	LIQUID	60		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52989-001	HAND SANITIZER LIQUID [TAIZHOU YADAI DAILY-USE CO., LTD.]	2	Legacy NDC, 1 package rows	20200415_a2c2df88-ebed-dfe4-e053-2995a90ae08b.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

hand sanitizer
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52989-001	52989-001-01

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
ALCOHOL	3K9958V90M	ACTIB
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
a34d0f54-8234-4443-e053-2995a90a123c			a2c2df88-ebed-dfe4-e053-2995a90ae08b	2020-04-14	Warnings	Exact identifier spl id: a34d0f54-8234-4443-e053-2995a90a123c spl set id: a2c2df88-ebed-dfe4-e053-2995a90ae08b

Reported adverse events (FAERS/openFDA)#

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