Natural Sun Aq Total Anti-aging Essence Sun
FDA Label NDC 51523-102

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Thefaceshop Co., Ltd for the product Natural Sun Aq Total Anti-aging Essence Sun (NDC 51523-102). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, otc - purpose, otc - when using, otc - stop use, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

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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