PK 99 Hand Sanitizer

Manufacturer: PHYLUS CO.,LTD
Effective date: 2020-07-27
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:22:42

Label at a glance#

ProductPK 99 Hand Sanitizer

Active ingredientALCOHOL

Label structure10 sections

Indications and uses

■ Hand sanitizer to help reduce bacteria that potentially can cause disease.

Dosage and administration

■ Place enough product on hands to cover all surfaces. Rub hands together until dry. ■ Supervise children under 6 years of age when using this product to avoid swallowing.

Contacts and useful links#

Websitewww.phylus.co.kr

www.phylus.co.kr

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Carbomer, Water, Glycerin

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame
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When using this product ■ do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water ■ avoid contact with broken skin ■ do not inhale or ingest
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Stop use and ask a doctor if irritation or rash appears and lasts

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

■ Hand sanitizer to help reduce bacteria that potentially can cause disease.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Place enough product on hands to cover all surfaces. Rub hands together until dry.
■ Supervise children under 6 years of age when using this product to avoid swallowing.

Other information

OTHER SAFETY INFORMATION

■ Store below 86℉(Between 1~30℃)
■ May discolor certain fabrics or surfaces

Questions?

OTC - QUESTIONS SECTION

■ www.phylus.co.kr , +82-43-421-0330

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of bottle

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
77448-030-01	2024-01-30	C162847	48780-1	1030e365-1cb3-111a-e063-dadaa90a10e2	99ea68d7-ac91-4c5e-a79b-53680df3f8f8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
77448-030-01	PK 99 Hand Sanitizer	3.78 L in 1 BOTTLE	GEL	3.78		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77448-030	PK 99 HAND SANITIZER (ALCOHOL) GEL [PHYLUS CO.,LTD]	2	Legacy NDC, 1 package rows	20200727_99ea68d7-ac91-4c5e-a79b-53680df3f8f8.zip

Products#

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

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

PK 99 Hand Sanitizer
Alcohol
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
WATER
Glycerin

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77448-030	77448-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
WATER	059QF0KO0R	IACT
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
5a069708-fe98-49dd-bc5d-2de4b5b8dc86			99ea68d7-ac91-4c5e-a79b-53680df3f8f8	2020-07-27	Warnings	Exact identifier spl id: 5a069708-fe98-49dd-bc5d-2de4b5b8dc86 spl set id: 99ea68d7-ac91-4c5e-a79b-53680df3f8f8

Reported adverse events (FAERS/openFDA)#

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