FOASU DAILY HAND SANITIZER gel

Manufacturer: HANSCOS Co.,Ltd.
Effective date: 2020-05-15
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:13:13

Label at a glance#

ProductFOASU DAILY HAND SANITIZER gel

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

Put nough produt in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product

Storage and handling

Store below 110°F (43°C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Put nough produt in your palm to cover hands and rub hands together briskly until dry.
Children under 6 years of age should be supervised when using this product

Other information

STORAGE AND HANDLING SECTION

Store below 110°F (43°C)
May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, GLYCERIN, PEG-60 HYDROGENATED CASTOR OIL, CARBOMER, TRIETHANOLAMINE, CAMELLIA SIMENSIS LEAF EXTRACT, ALOE BARBADENSIS LEAF EXTRACT, MENTHA PIPERITA (PEPPERMINT) OIL, LIMONENE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product Label

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
77964-001-01	2021-07-23	C162847	48780-1	c7ccaba7-13ef-fd44-e053-dadaa90aa01b	FOASU DAILY HAND SANITIZER GEL
77964-001-02	2021-07-23	C162847	48780-1	c7ccaba7-13ef-fd44-e053-dadaa90aa01b	FOASU DAILY HAND SANITIZER GEL
77964-001-03	2021-07-23	C162847	48780-1	c7ccaba7-13ef-fd44-e053-dadaa90aa01b	FOASU DAILY HAND SANITIZER GEL
77964-001-04	2021-07-23	C162847	48780-1	c7ccaba7-13ef-fd44-e053-dadaa90aa01b	FOASU DAILY HAND SANITIZER GEL
77964-001-05	2021-07-23	C162847	48780-1	c7ccaba7-13ef-fd44-e053-dadaa90aa01b	FOASU DAILY HAND SANITIZER GEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
77964-001-01	FOASU DAILY HAND SANITIZER gel	30 mL in 1 TUBE	GEL	30	1
77964-001-02	FOASU DAILY HAND SANITIZER gel	50 mL in 1 TUBE	GEL	50	1
77964-001-03	FOASU DAILY HAND SANITIZER gel	100 mL in 1 TUBE	GEL	100	1
77964-001-04	FOASU DAILY HAND SANITIZER gel	250 mL in 1 BOTTLE, PUMP	GEL	250	1
77964-001-05	FOASU DAILY HAND SANITIZER gel	500 mL in 1 BOTTLE, PUMP	GEL	500	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
77964-001	FOASU DAILY HAND SANITIZER GEL (ALCOHOL) GEL [HANSCOS CO.,LTD.]	1	Legacy NDC, 5 package rows	20200516_19f72eab-665c-48a7-ab6d-e24b9fead417.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

FOASU DAILY HAND SANITIZER gel
alcohol
WATER
GLYCERIN
PEG-60 HYDROGENATED CASTOR OIL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
TROLAMINE
GREEN TEA LEAF
ALOE VERA LEAF
PEPPERMINT OIL
LIMONENE, (+)-

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77964-001	77964-001-01, 77964-001-02, 77964-001-03, 77964-001-04, 77964-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
PEG-60 HYDROGENATED CASTOR OIL	02NG325BQG	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
TROLAMINE	9O3K93S3TK	IACT
GREEN TEA LEAF	W2ZU1RY8B0	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
PEPPERMINT OIL	AV092KU4JH	IACT
LIMONENE, (+)-	GFD7C86Q1W	IACT
ALCOHOL	3K9958V90M	ACTIB

Source Document#

Source XML · Source PDF

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
a5b3f500-d573-970c-e053-2995a90a82e6			19f72eab-665c-48a7-ab6d-e24b9fead417	2020-05-15	Warnings	Exact identifier spl id: a5b3f500-d573-970c-e053-2995a90a82e6 spl set id: 19f72eab-665c-48a7-ab6d-e24b9fead417

Reported adverse events (FAERS/openFDA)#

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