Duride Hand Sanitizer

Manufacturer: Rainbow International Services Inc. | Guangzhou Pinshang Biotechnology Development Co.,Ltd
Effective date: 2020-05-11
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:11:00

Label at a glance#

ProductDuride Hand Sanitizer

Active ingredientALCOHOL

Label structure12 sections

Storage and handling

Store below 110℉(43℃)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

Water(Aqua), Glycerin, Carbomer, Aloe Barbadensis Leaf Juice(Aloe Vera), Tocopheryl Acetate(Vitamin E), Phenoxyethanol, Aminomethyl propanol

OTC - PURPOSE SECTION

Antimicrobial

INDICATIONS & USAGE SECTION

■ Hand sanitizer to help reduce bacteria on the skin.

WARNINGS SECTION

■ Flammable. Keep away from fire or flame.

■ For external use only.

OTC - DO NOT USE SECTION

■ in children less than 2 months of age
■ on open skin wounds

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.

STORAGE AND HANDLING SECTION

Store below 110℉(43℃)

DOSAGE & ADMINISTRATION SECTION

Pump 1-2 times and rub it into your hand. For topical use only.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Duride Hand Sanitizer 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
77498-210-01	2022-01-28	C162847	48780-1	d6a99b39-d91f-a426-e053-dadaa90af4c2	a56b7369-c972-4dcc-e053-2a95a90a638b
77498-210-02	2022-01-28	C162847	48780-1	d6a99b39-d91f-a426-e053-dadaa90af4c2	a56b7369-c972-4dcc-e053-2a95a90a638b
77498-210-03	2022-01-28	C162847	48780-1	d6a99b39-d91f-a426-e053-dadaa90af4c2	a56b7369-c972-4dcc-e053-2a95a90a638b
77498-210-04	2022-01-28	C162847	48780-1	d6a99b39-d91f-a426-e053-dadaa90af4c2	a56b7369-c972-4dcc-e053-2a95a90a638b

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
77498-210-01	Duride Hand Sanitizer	60 mL in 1 BOTTLE, PLASTIC	GEL	60	1
77498-210-02	Duride Hand Sanitizer	250 mL in 1 BOTTLE, PUMP	GEL	250	1
77498-210-03	Duride Hand Sanitizer	300 mL in 1 BOTTLE, PUMP	GEL	300	1
77498-210-04	Duride Hand Sanitizer	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
77498-210	DURIDE HAND SANITIZER (ALCOHOL) GEL [RAINBOW INTERNATIONAL SERVICES INC.]	1	Legacy NDC, 4 package rows	20200513_a56b7369-c972-4dcc-e053-2a95a90a638b.zip

Products#

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

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

Duride Hand Sanitizer
Alcohol
WATER
GLYCERIN
ALOE VERA LEAF
CARBOMER 940
AMINOMETHYLPROPANOL
.ALPHA.-TOCOPHEROL ACETATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
77498-210	77498-210-01, 77498-210-02, 77498-210-03, 77498-210-04

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
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
ALOE VERA LEAF	ZY81Z83H0X	IACT
CARBOMER 940	4Q93RCW27E	IACT
ALCOHOL	3K9958V90M	ACTIB
AMINOMETHYLPROPANOL	LU49E6626Q	IACT
.ALPHA.-TOCOPHEROL ACETATE	9E8X80D2L0	IACT

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
a56b7369-c973-4dcc-e053-2a95a90a638b			a56b7369-c972-4dcc-e053-2a95a90a638b	2020-05-11	Warnings	Exact identifier spl id: a56b7369-c973-4dcc-e053-2a95a90a638b spl set id: a56b7369-c972-4dcc-e053-2a95a90a638b

Reported adverse events (FAERS/openFDA)#

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