HAND SANITIZER- alcohol liquid

hand sanitizer by

Drug Labeling and Warnings

hand sanitizer by is a Otc medication manufactured, distributed, or labeled by ningbo fareast industry co.,ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

ACTIVE INGREDIENT

PURPOSE

INDICATIONS & USAGE

to help reduce bacteria that potentially can cause disease.for use when soap and water are not available

WARNINGS

for external use only,flammable,keep away from heat or flame

DO NOT USE

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

WHEN USING

when using this product keep out of eyes,ears,and mouth in case of contact with eyes,rinse eyes thorough with water
stop use and ask a doctor if irritation or rash occurs,these may be signs of a serious condition.
keep out of reach of children,if swallowed,get medical help or contact a poison control center right away.

STOP USE

stop use and ask a doctor if irriation or rash occurs,these may be signs of a serious condition

KEEP OUT OF REACH OF CHILDREN

keep out of reach of children ,if swallowed, get medical help or contact a posion control center right away .

DOSAGE & ADMINISTRATION

place enough product on hands to cover all surface,rub hands together until dry
supervise children under 6 years when using this product to avoid swallowing

STORAGE AND HANDLING

INACTIVE INGREDIENT

PRINCIPAL DISPLAY PANEL

20ML NDC 78623-016-20

30ML NDC 78623-016-30

60ML NDC 78623-016-60

75ML NDC 78623-016-75

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78623-016
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78623-016-20	20 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/11/2021
2	NDC: 78623-016-30	30 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/11/2021
3	NDC: 78623-016-60	60 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/11/2021
4	NDC: 78623-016-75	75 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/11/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	12/10/2020

Labeler - ningbo fareast industry co.,ltd (554535808)