WALLY Hand Sanitizer Gel

Manufacturer: Ester Co., Ltd.
Effective date: 2020-05-21
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:14:05

Label at a glance#

ProductWALLY Hand Sanitizer Gel

Active ingredientALCOHOL

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

WALLY Hand Sanitizer Gel

OTC - ACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - PURPOSE SECTION

INDICATIONS & USAGE SECTION

INACTIVE INGREDIENT SECTION

OTC - DO NOT USE SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - WHEN USING SECTION

INSTRUCTIONS FOR USE SECTION

WARNINGS SECTION

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
74004-703-01	2022-01-28	C162847	48780-1	d6a99b39-d946-a426-e053-dadaa90af4c2	[Ester Co., Ltd.-WALLY Hand Sanitizer Gel] 500 ml : BOTTLE+PUMP : 74004-703-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74004-703-01	WALLY Hand Sanitizer Gel	500 mL in 1 BOTTLE, PUMP	GEL	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74004-703	WALLY HAND SANITIZER GEL (ALCOHOL) GEL [ESTER CO., LTD.]	1	Legacy NDC, 1 package rows	20200521_a62507d9-048e-139f-e053-2995a90a2bc9.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

WALLY Hand Sanitizer Gel
ALCOHOL
ALLANTOIN
GREEN TEA LEAF
BUTYLENE GLYCOL
EDETOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
ALOE ARBORESCENS LEAF
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74004-703	74004-703-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALLANTOIN	344S277G0Z	IACT
GREEN TEA LEAF	W2ZU1RY8B0	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
EDETOL	Q4R969U9FR	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
ALOE ARBORESCENS LEAF	09TD8L5SQV	IACT
ALCOHOL	3K9958V90M	ACTIB
GLYCERIN	PDC6A3C0OX	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
a62507d9-048f-139f-e053-2995a90a2bc9			a62507d9-048e-139f-e053-2995a90a2bc9	2020-05-21		Exact identifier spl id: a62507d9-048f-139f-e053-2995a90a2bc9 spl set id: a62507d9-048e-139f-e053-2995a90a2bc9

Reported adverse events (FAERS/openFDA)#

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