DR.CLEANEW HAND SANITIZER- alcohol liquid

Dr.Cleanew Hand Sanitizer by

Drug Labeling and Warnings

Dr.Cleanew Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by NR CO.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PURPOSE

Antimicrobial

Active Ingredients

ALCOHOL

Use

Hand sanitizer to help reduce bacteria that potentially can cause disease.
Recommended for external use only.

Warnings

For external use only

Keep away from fire of flame

Do not spray on clothes because it can stain.

Be caeful not to get into your eyes, and if so wash thoroughly with water

Keep out of reach of children

Keep out of reach of children.

Stop use and ask a doctor

Take care not to get into the eye.

If a children has swallowed it go to the hospital immediately and see a doctor

Other information

beause replacing in other containers can cause accidents or deteriorate quality, put it in the original container and keep

it tightly closed.

store away from high temperature and fire.

indication

sprinkle evenly on your hands

do not use

do not use on intraoral, mucosal and damaged skin

carefully use for the people with allergic reactions,

immediately discontinue use and consult a dermatologist if hypersensitivity symptoms

such as rash itching etc occur

skin irritation symptoms occur

inactive ingredient

water, citric acid

Direction

disinfection of hands and skin

Spray on hands or spray where disinfection is needed

label

79191-301-01

79191-301-02

INGREDIENTS AND APPEARANCE

DR.CLEANEW HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 79191-301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	60 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)	0.5 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	39.5 mL  in 100 mL

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 79191-301-01	100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/25/2020
2	NDC: 79191-301-02	500 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/25/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/25/2020

Labeler - NR CO.,Ltd. (690430136)

Registrant - NR CO.,Ltd. (690430136)

Establishment
Name	Address	ID/FEI	Business Operations
NR CO.,Ltd.		690430136	manufacture(79191-301)