OULL FRESH PURE HAND Gel

Manufacturer: Ester Co., Ltd.
Effective date: 2020-11-11
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:33:36

Label at a glance#

ProductOULL FRESH PURE HAND Gel

Active ingredientALCOHOL

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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	2
581662	ethanol 0.7 ML/ML Topical Gel	SCD	2
581662	ethanol 70 % Topical Gel	SY	2
581662	ethyl alcohol 70 % Topical Gel	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74004-137-20	2022-01-28	C162847	48780-1	d6a99b39-ffa1-a426-e053-dadaa90af4c2	[Ester Co., Ltd.-OULL FRESH PURE HAND GEL] 30 ml X 20 : 74004-137-20

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74004-137-20	OULL FRESH PURE HAND Gel	20 in 1 BOX	GEL	20		2
74004-137-20	OULL FRESH PURE HAND Gel	30 mL in 1 POUCH	GEL	30		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74004-137	OULL FRESH PURE HAND GEL (ALCOHOL) GEL [ESTER CO., LTD.]	2	Legacy NDC, 2 package rows	20201114_a3bbca4b-3136-69f6-e053-2a95a90a7c77.zip

Products#

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

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

OULL FRESH PURE HAND Gel
ALCOHOL
POLYSORBATE 60
BUTYLENE GLYCOL
ISOPROPYL MYRISTATE
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
TROLAMINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74004-137	74004-137-20

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
POLYSORBATE 60	CAL22UVI4M	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
TROLAMINE	9O3K93S3TK	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
b3e0bc1d-2129-c005-e053-2a95a90a89d6			a3bbca4b-3136-69f6-e053-2a95a90a7c77	2020-11-11		Exact identifier spl id: b3e0bc1d-2129-c005-e053-2a95a90a89d6 spl set id: a3bbca4b-3136-69f6-e053-2a95a90a7c77

Reported adverse events (FAERS/openFDA)#

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