HAND SANITIZER 3.4OZ 01- alcohol liquid

hand sanitizer 3.4oz by

Drug Labeling and Warnings

hand sanitizer 3.4oz by is a Otc medication manufactured, distributed, or labeled by Shenzhen Lantern Scicence Co Ltd, Lantern Beauty America,INC., Shenzhen Lantern Science Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Active Ingredient purpose

Ethyl Alcohol 75%( v/v) Antiseptic

USE

Hand sanitizer to help reduce bacteria that potentiallycan cause disease.For use when soap and water are not available.

Recommended for repeated use.

use anywhere without water.

Warning

For external use only.

Flammable, keep away from heat and flame.

Discontinue if skin becomes irritated and ask a doctor .

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a poson control center immediately.

Inavtive ingredients

Water, Glycerin,Propylene Glycol,Carbomer,,Aminomethyl propanol,Fragrance(parfum).

Directions

place enough product on hands to cover all surfaces,Rub hands together until dry.

supervise children under 6 years of age when using this product to avoid swallowing.

When using this product

keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Do not inhale or ingest.

Avoid contact with broken skin.

Other information

Do not store above 105F.

May discolor some fabrics.

Harmful to wood finishes and plastics.

Do not use

In children less than 2 months of age or on open wounds

when using this product

keep out of eyes,ears and mouth,in case of contact with eyes,rinse eyes thoroughly 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.

other information

between 15-30℃（59-86℉）。Avoid freezing and excessive heat above 40℃（104℉）.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HAND SANITIZER 3.4OZ  01
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-219
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
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.01 mL  in 100 mL
LEMON (UNII: 24RS0A988O)	0.1 mL  in 100 mL
CARBOMER 940 (UNII: 4Q93RCW27E)	0.35 mL  in 100 mL
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)	0.11 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	28.42 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.01 mL  in 100 mL

Product Characteristics
Color	white (transparant)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54860-219-01	100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/22/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/22/2020

Labeler - Shenzhen Lantern Scicence Co Ltd (421222423)

Registrant - Lantern Beauty America,INC. (117371139)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Lantern Science Co.,Ltd.		421222423	manufacture(54860-219)