DURIDE HAND SANITIZER- alcohol gel

Duride Hand Sanitizer by

Drug Labeling and Warnings

Duride Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Rainbow International Services Inc., Guangzhou Pinshang Biotechnology Development Co.,Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Alcohol

INACTIVE INGREDIENT

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

PURPOSE

Antimicrobial

INDICATIONS & USAGE

■ Hand sanitizer to help reduce bacteria on the skin.

WARNINGS

■ Flammable. Keep away from fire or flame.

■ For external use only.

DO NOT USE

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

WHEN USING

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

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

STORAGE AND HANDLING

Store below 110℉(43℃)

DOSAGE & ADMINISTRATION

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DURIDE HAND SANITIZER 
alcohol gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 77498-210
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	210 mL  in 300 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CARBOMER 940 (UNII: 4Q93RCW27E)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 77498-210-01	60 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/12/2020
2	NDC: 77498-210-02	250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/12/2020
3	NDC: 77498-210-03	300 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/12/2020
4	NDC: 77498-210-04	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/12/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/12/2020

Labeler - Rainbow International Services Inc. (046587936)

Registrant - Rainbow International Services Inc. (046587936)

Establishment
Name	Address	ID/FEI	Business Operations
Rainbow International Services Inc.		046587936	label(77498-210)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Pinshang Biotechnology Development Co.,Ltd		554530020	manufacture(77498-210)