Dr. Barrier Intensive Hand Sanitizer Gel

Manufacturer: SISKINKOREA CO.,LTD.
Effective date: 2020-08-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:24:31

Label at a glance#

ProductDr. Barrier Intensive Hand Sanitizer Gel

Active ingredientALCOHOL

Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dr Barrier Intensive Hand Santizer Gel

WARNINGS SECTION

OTC - ACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTION

DOSAGE & ADMINISTRATION SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - DO NOT USE SECTION

OTC - PURPOSE SECTION

OTC - STOP USE SECTION

INDICATIONS & USAGE 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
74514-0801-1	2023-01-30	C162847	48780-1	f386c649-b57a-0266-e053-dadaa90a7c1a	Dr. Barrier Intensive Hand Sanitizer Gel \| 3785 mL \| 74514-0801-1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74514-0801-1	Dr. Barrier Intensive Hand Sanitizer Gel	3785 mL in 1 BOTTLE	GEL	3785		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74514-0801	DR. BARRIER INTENSIVE HAND SANITIZER GEL (ALCOHOL) GEL [SISKINKOREA CO.,LTD.]	1	Legacy NDC, 1 package rows	20200812_acaa36b2-c17d-6337-e053-2995a90aa545.zip

Products#

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

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

Dr. Barrier Intensive Hand Sanitizer Gel
Alcohol
GLYCERIN
.ALPHA.-TOCOPHEROL ACETATE
EDETOL
WATER
HYALURONATE SODIUM
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74514-0801	74514-0801-1

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
GLYCERIN	PDC6A3C0OX	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT
EDETOL	Q4R969U9FR	IACT
WATER	059QF0KO0R	IACT
HYALURONATE SODIUM	YSE9PPT4TH	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	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
acaa0a63-e3e0-6486-e053-2995a90acfd1			acaa36b2-c17d-6337-e053-2995a90aa545	2020-08-12		Exact identifier spl id: acaa0a63-e3e0-6486-e053-2995a90acfd1 spl set id: acaa36b2-c17d-6337-e053-2995a90aa545

Reported adverse events (FAERS/openFDA)#

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