KEKE HAND SANITIZER 500ML 01- alcohol liquid

KEKE hand sanitizer 500ml by

Drug Labeling and Warnings

KEKE hand sanitizer 500ml 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

keep out of reach of children

If swallowed,get medical help or contact a Poison Control Center right away.

Recommended for repeated use.

use anywhere without water.

Warning

For external use only:hands

Flammable,keep away from fire or flame.

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.

Inactive ingredients

Aqua,Glycerin,Aloe Yohjyu Matsu Ekisu,Tocopheryl Acetate,Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Aminomethyl Propanol,Parfum.

Directions

put a thumbnail size amount in your palm and rub your hands together briskly until dry.Children under 6 years of age should be supervised when using this product.Not recommended for infants.

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.

Other information

Do not store above 100℉（38℃)

Harmful to wood finishes and plastics.

Purpose

Antiseptic

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

KEKE HAND SANITIZER 500ML  01
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-259
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
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	0.01 mL  in 100 mL
ALOE ANDONGENSIS WHOLE (UNII: XOQ5N25YKS)	0.01 mL  in 100 mL
ALOE (UNII: V5VD430YW9)	0.15 mL  in 100 mL
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)	0.3 mL  in 100 mL
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)	0.09 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	23.85 mL  in 100 mL
GLYCERIN (UNII: PDC6A3C0OX)	0.5 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: 54860-259-01	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/09/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/09/2020

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(54860-259)