ECO 10 MINERAL SUN PRO PUFF TYPE- zinc oxide powder

ECO 10 Mineral Sun Pro Puff type by

Drug Labeling and Warnings

ECO 10 Mineral Sun Pro Puff type by is a Otc medication manufactured, distributed, or labeled by MIZON CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

zinc oxide

INACTIVE INGREDIENT

Mica,Silica ,Triethoxycaprylylsilane,Iron Oxides,Dimethicone,Aluminum Hydroxide,Glycerine,
Iron Oxides,Methicone,Bismuth Oxychloride,Iron Oxides,Hydrolyzed Algin,Laminaria Digitata Extract,
Phormidium Persicinum Extract,Undaria Pinnatifida Extract  ,Plankton extract,Phenethyl Alcohol  ,
Chlorella vulgaris extract,Pancratium maritimum extract,Crithmum Maritimum Extract,
Helichrysum italicum extract, Ulex europaeus leaf/root/stem extract

PURPOSE

UVA/UVB protection

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

Apply it to your face after all of your basic skincare. If you need better UV protect effect, apply it more whenever and wherever needed

WARNINGS

1. If following symptoms occur, stop use and consult a doctor : red spots, swelling, itcihng, irritation, or symtoms on applied skin under direct sunlight.
2. Do not use on scarred skin, or if you have dermatitis or eczema
3. Keep the cap close on its product
4. Keep away from direct sunlight or heat.
5. This product blocks UVA rays and ultraviolet protection effectiveness have been measured by the Food and Drug Administration methods and standards

DOSAGE & ADMINISTRATION

for topical use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ECO 10 MINERAL SUN PRO PUFF TYPE 
zinc oxide powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 57718-040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Zinc oxide (UNII: SOI2LOH54Z) (Zinc oxide - UNII:SOI2LOH54Z)	Zinc oxide	15.004 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE (UNII: 92RU3N3Y1O)
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
GLYCERIN (UNII: PDC6A3C0OX)
BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57718-040-01	12 g in 1 CONTAINER

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	07/03/2014

Labeler - MIZON CO., LTD. (557815570)

Registrant - MIZON CO., LTD. (557815570)

Establishment
Name	Address	ID/FEI	Business Operations
MIZON CO., LTD.		557815570	manufacture(57718-040)