NIMBUS 9 HAND SANITIZER 3.78L 01- alcohol liquid

Nimbus9 hand sanitizer 3.78L by

Drug Labeling and Warnings

Nimbus9 hand sanitizer 3.78L 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 71%（w/w） Antiseptic

USE

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

Recommended for repeated use.

use anywhere without water.

Warning

For external use only-hands.

Flammable,keep away from heat and 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

Water(Aqua),Glycerin,Propylene Glycol,Carbomer,Aminomethyl Propanol,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.

Keep out of reach of children

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

Do not use

in children less than 2 months of age.

on open skin wounds.

Stop use and ask a doctor

if irritation or rash occurs,these maybe signs of a serious condition.

Other information

Store between 15-30 C（59-86F）

Avoid freezing and excessive heat above 40C(104F）

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NIMBUS 9 HAND SANITIZER 3.78L  01
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-263
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	71 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LEMON (UNII: 24RS0A988O)	0.1 g  in 100 g
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.01 g  in 100 g
CARBOMER 940 (UNII: 4Q93RCW27E)	0.35 g  in 100 g
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)	0.11 g  in 100 g
WATER (UNII: 059QF0KO0R)	28.42 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	0.01 g  in 100 g

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: 54860-263-01	3780 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/11/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/11/2020

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(54860-263)