advanced hand sanitizer

Manufacturer: Guangzhou Fuda Biotechnology Co., Ltd.
Effective date: 2020-04-20
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:08:31

Label at a glance#

Productadvanced hand sanitizer

Active ingredientALCOHOL

Label structure11 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin.

Dosage and administration

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

Storage and handling

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75%(v/v)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

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

When using this product

OTC - WHEN USING SECTION

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/or 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

Directions

DOSAGE & ADMINISTRATION SECTION

Put enough product in your palm to cover both hands and rub hands together briskly until dry.

Children under 6 years of age should be supervised when using this.

Other information

STORAGE AND HANDLING SECTION

Store below 110°F(43℃)

May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Glycerin,Carbomer,Aminomethyl Propanol, Vitamin E

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50 ml label60 ml label100 ml label200 ml label300 ml label500 ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1305100	ethanol 75 % Topical Gel	PSN	1
1305100	ethanol 0.75 ML/ML Topical Gel	SCD	1
1305100	ethanol 75 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
75151-001-01	2021-07-23	C162847	48780-1	c7ccaba7-1722-fd44-e053-dadaa90aa01b	ADVANCED HAND SANITIZER
75151-001-02	2021-07-23	C162847	48780-1	c7ccaba7-1722-fd44-e053-dadaa90aa01b	ADVANCED HAND SANITIZER
75151-001-03	2021-07-23	C162847	48780-1	c7ccaba7-1722-fd44-e053-dadaa90aa01b	ADVANCED HAND SANITIZER
75151-001-04	2021-07-23	C162847	48780-1	c7ccaba7-1722-fd44-e053-dadaa90aa01b	ADVANCED HAND SANITIZER
75151-001-05	2021-07-23	C162847	48780-1	c7ccaba7-1722-fd44-e053-dadaa90aa01b	ADVANCED HAND SANITIZER
75151-001-06	2021-07-23	C162847	48780-1	c7ccaba7-1722-fd44-e053-dadaa90aa01b	ADVANCED HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
75151-001-01	advanced hand sanitizer	50 mL in 1 AMPULE	GEL	50	1
75151-001-02	advanced hand sanitizer	60 mL in 1 AMPULE	GEL	60	1
75151-001-03	advanced hand sanitizer	100 mL in 1 AMPULE	GEL	100	1
75151-001-04	advanced hand sanitizer	200 mL in 1 AMPULE	GEL	200	1
75151-001-05	advanced hand sanitizer	300 mL in 1 AMPULE	GEL	300	1
75151-001-06	advanced hand sanitizer	500 mL in 1 AMPULE	GEL	500	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75151-001	ADVANCED HAND SANITIZER GEL [GUANGZHOU FUDA BIOTECHNOLOGY CO., LTD.]	1	Legacy NDC, 6 package rows	20200429_a3b73729-24ce-e3ea-e053-2a95a90ae622.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

advanced hand sanitizer
GLYCERIN
ALCOHOL
AMINOMETHYLPROPANOL
.ALPHA.-TOCOPHEROL
WATER
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75151-001	75151-001-01, 75151-001-02, 75151-001-03, 75151-001-04, 75151-001-05, 75151-001-06

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
ALCOHOL	3K9958V90M	ACTIB
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
.ALPHA.-TOCOPHEROL	H4N855PNZ1	IACT
WATER	059QF0KO0R	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	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
a3b54bee-e65f-216b-e053-2a95a90aca1c			a3b73729-24ce-e3ea-e053-2a95a90ae622	2020-04-20	Warnings	Exact identifier spl id: a3b54bee-e65f-216b-e053-2a95a90aca1c spl set id: a3b73729-24ce-e3ea-e053-2a95a90ae622

Reported adverse events (FAERS/openFDA)#

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