Otc - Active Ingredient
OCTINOXATE (7.50%) OCTISALATE (3.00%)TITANIUM DIOXIDE (2.34%)AVOBENZONE (2.30%)ENZACAMENE (2.00%)
Natural Sun Aq Body And Family Mild Sun Milk
FDA Label NDC 51523-101
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 Body And Family Mild Sun Milk (NDC 51523-101). 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
Inactive Ingredient
WATER · CYCLOMETHICONE · GLYCERIN · DIPROPYLENE GLYCOL · DICAPRYLYL CARBONATE · OCTYLDODECYL NEOPENTANOATE · POTASSIUM CETYL PHOSPHATE · SORBITAN MONOSTEARATE · GLYCERYL MONOSTEARATE · POLYOXYL 100 STEARATE · DIMETHICONE · CETEARYL ALCOHOL · COPTIS · MINERAL OIL ·XANTHAN GUM · STEARIC ACID · ALOE FEROX LEAF · SILICON DIOXIDE · EDETATE DISODIUM · IONONE · BENZYL BENZOATE · BUTYLPHENYL METHYLPROPIONAL · .ALPHA.-HEXYLCINNAMALDEHYDE
Otc - Purpose
Face and Body 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 parts easily exposed to UV rays such as the face, neck, arms and legs)
Package Label.Principal Display Panel
NATURAL SUN AQ BODY AND FAMILY MILD SUN MILK
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