FDA Label for Natural Sun Aq Total Anti-aging Essence Sun
View Indications, Usage & Precautions
Natural Sun Aq Total Anti-aging Essence Sun Product Label
The following document was submitted to the FDA by the labeler of this product Thefaceshop Co., Ltd. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
OCTINOXATE (7.50%) OCTISALATE (3.00%)TITANIUM DIOXIDE (2.34%)AVOBENZONE (2.30%)ENZACAMENE (2.00%)NIACINAMIDE (2.00%)ADENOSINE (0.04%)
Inactive Ingredient
WATER ∙ CYCLOMETHICONE ∙ DIPROPYLENE GLYCOL ∙ POTASSIUM CETYL PHOSPHATE ∙ DICAPRYLYL CARBONATE ∙ OCTYLDODECYL NEOPENTANOATE ∙ GLYCERIN ∙ STEARIC ACID ∙ GLYCOL STEARATE ∙ POLYOXYL 100 STEARATE ∙ CETEARYL ALCOHOL ∙ GLYCERYL STEARATE ∙ XANTHAN GUM ∙ SILICON DIOXIDE ∙ SORBITAN MONOSTEARATE ∙ MINERAL OIL ∙ TROLAMINE ∙ EDETATE DISODIUM ∙ FERRIC OXIDE RED ∙ FERRIC OXIDE YELLOW ∙ METHYLPARABEN ∙ BENZYL BENZOATE ∙ BUTYLPHENYL METHYLPROPIONAL ∙ .ALPHA.-HEXYLCINNAMALDEHYDE
Otc - Purpose
Anti Aging Essence Sun Block
Otc - When Using
Avoid contact with eyes.
Otc - Stop Use
Discontinue use if sign of irritation or rash appear.
Dosage & Administration
Dispense an adequate amount and apply evenly. (At the final stage of basic skincare, dispense an adequate amount and apply evenly to desired parts)
Package Label.Principal Display Panel
NATURAL SUN AQ TOTAL ANTI-AGING ESSENCE SUN
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