MEDIPLUS Hand Sanitizer

Manufacturer: GL Pharm Co Ltd
Effective date: 2020-04-09
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:05:41

Label at a glance#

ProductMEDIPLUS Hand Sanitizer

Active ingredientBENZALKONIUM CHLORIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

benzaklonium chloride 0.66%

INACTIVE INGREDIENT SECTION

polyoxyethylene lauryl ether, ethanol, purified water

OTC - PURPOSE SECTION

hand sanitizer

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hands and fingers. Rub onto hands until dry.

Supervise children in the use of this product.

WARNINGS SECTION

■ Flammable. Keep away from fire or flame.

■ For external use only.

■ Do not use in eyes.

■ lf swallowed, get medical help promptly.

■ Stop use, ask doctor lf irritation occurs.

■ Keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
74713-0001-1	2021-07-23	C162847	48780-1	c7ccaba7-2529-fd44-e053-dadaa90aa01b	Drug Facts
74713-0001-2	2021-07-23	C162847	48780-1	c7ccaba7-2529-fd44-e053-dadaa90aa01b	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
74713-0001-1	MEDIPLUS Hand Sanitizer	300 mL in 1 BOTTLE	LIQUID	300		1
74713-0001-2	MEDIPLUS Hand Sanitizer	100 mL in 1 BOTTLE	LIQUID	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
74713-0001	MEDIPLUS HAND SANITIZER (BENZALKONIUM CHLORIDE) LIQUID [GL PHARM CO LTD]	1	Legacy NDC, 2 package rows	20200410_a2da50a7-de8c-6204-e053-2a95a90a5e2b.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

MEDIPLUS Hand Sanitizer
benzalkonium chloride
WATER
BENZALKONIUM
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
74713-0001	74713-0001-1, 74713-0001-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
BENZALKONIUM CHLORIDE	F5UM2KM3W7	ACTIB
ALCOHOL	3K9958V90M	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
a2da505a-98a7-9bae-e053-2995a90a9a3c			a2da50a7-de8c-6204-e053-2a95a90a5e2b	2020-04-09	Warnings	Exact identifier spl id: a2da505a-98a7-9bae-e053-2995a90a9a3c spl set id: a2da50a7-de8c-6204-e053-2a95a90a5e2b

Reported adverse events (FAERS/openFDA)#

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