MELLOW HAND SANITIZER 59ML ML315 01- alcohol liquid

Mellow hand sanitizer 59ml ML315 by

Drug Labeling and Warnings

Mellow hand sanitizer 59ml ML315 by is a Otc medication manufactured, distributed, or labeled by Shenzhen Lantern Scicence Co.,Ltd., LANTERN HEALTH&BEAUTY LAB INC., Shenzhen Lantern Science Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Active Ingredient purpose

Alcohol 62% v/v Antiseptic

Features

To decrease bacteria on the skin that could cause disease

Recommended for repeated use.

Use anywhere without water

Recommended for repeated use.

use anywhere without water.

Warning

For external use only

Flammable,keep away from fire or 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 Poison control Center immediately.

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(Water), Glycerin,Isopropyl Myristate,Propylene Glycol,Tocopheryl Acetate,Aminomethyl propanol,Carbomer,parfum.

Directions

wet hands thoroughly with product and rub until dry without wiping.

For children under 6,use only under adult supervision.

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.

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.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MELLOW HAND SANITIZER 59ML ML315  01
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54860-275
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	62 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)	0.0001 mL  in 100 mL
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)	0.001 mL  in 100 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	0.01 mL  in 100 mL
LEMON (UNII: 24RS0A988O)	0.1 mL  in 100 mL
CARBOMER 940 (UNII: 4Q93RCW27E)	26 mL  in 100 mL
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)	0.08 mL  in 100 mL
WATER (UNII: 059QF0KO0R)	37.5398 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: 54860-275-01	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/14/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	05/14/2020

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(54860-275)