be Flat. Frecent HAND SANITIZER

Manufacturer: YOON JI CORPORATION CO.,LTD
Effective date: 2020-07-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:19:58

Label at a glance#

Productbe Flat. Frecent HAND SANITIZER

Active ingredientALCOHOL

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

be Flat Frecent HAND SANITIZER single use

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
75024-715-01	2024-01-30	C162847	48780-1	1030e365-4822-111a-e063-dadaa90a10e2	be Flat. Frecent HAND SANITIZER 1.5 ml x 1: 75024-715-01

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75024-715-01	be Flat. Frecent HAND SANITIZER	1.5 mL in 1 POUCH	GEL	1.5		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75024-715	BE FLAT. FRECENT HAND SANITIZER (ETHYL ALCOHOL) GEL [YOON JI CORPORATION CO.,LTD]	1	Legacy NDC, 1 package rows	20200703_a97228cf-b1e2-25fd-e053-2995a90a95ed.zip

Products#

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

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

be Flat. Frecent HAND SANITIZER
Ethyl Alcohol
BUTYLENE GLYCOL
ALOE VERA LEAF
GLYCERIN
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
PANTHENOL
TROLAMINE
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75024-715	75024-715-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
BUTYLENE GLYCOL	3XUS85K0RA	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
GLYCERIN	PDC6A3C0OX	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
PANTHENOL	WV9CM0O67Z	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
a971e5aa-3c6a-20c6-e053-2995a90a8f65			a97228cf-b1e2-25fd-e053-2995a90a95ed	2020-07-02		Exact identifier spl id: a971e5aa-3c6a-20c6-e053-2995a90a8f65 spl set id: a97228cf-b1e2-25fd-e053-2995a90a95ed

Reported adverse events (FAERS/openFDA)#

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