ECO 10 Mineral Sun Pro Puff type

Label at a glance#

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

zinc oxide

INACTIVE INGREDIENT SECTION

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

OTC - PURPOSE SECTION

UVA/UVB protection

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

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 SECTION

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 SECTION

for topical use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

DailyMed Dashboard NDC Coverage#

DailyMed Socrata Ingredients#

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

• ECO 10 Mineral Sun Pro Puff type
• Zinc oxide
• DIMETHICONE
• ALUMINUM HYDROXIDE
• HYALURONATE SODIUM
• GLYCERIN
• BISMUTH OXYCHLORIDE

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 2 · 84 matching rows.

openFDA label cross-check#

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Matched openFDA labels page 1 of 1 · 1 matching rows.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.