Active Ingredient
Active ingredients: Ethylhexyl Methoxycinnamate 7.0%, Homosalate 6.0%, Ethylhexyl Salicylate 4.5%
Tonymoly Bcdation Multi Use Sun
FDA Label NDC 59078-323
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tonymoly Co.,ltd for the product Tonymoly Bcdation Multi Use Sun (NDC 59078-323). 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 active ingredient, inactive ingredient, purpose, warnings, description, 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
Inactive Ingredients: Caprylic/Capric Triglyceride, Octyldodecyl Myristate, Dimethicone, Phenyl Trimethicone, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Methyl Trimethicone, Glyceryl Caprylate, Fragrance, Caprylyl Glycol, Rosa Centifolia Flower Oil, Calendula Officinalis Flower Oil, Cocos Nucifera (Coconut) Oil, Rubus Idaeus (Raspberry) Seed Oil, Polyglyceryl-2 Triisostearate, Water, Methylpropanediol, Propanediol, Polyglyceryl-4 Caprate, Polyglyceryl-2 Dipolyhydroxystearate
Purpose
Purpose: Sunscreen
Warnings
Warnings: For external use only. Avoid contact with eyes. Keep out of reach of children. Discontinue use if signs of irritation and/or rash appear. Do not use on - deep puncture wounds - animal bites - serious burns
Description
Use: Helps prevent sunburn - if used as directed with other sun protection measures.
Directions: Use at the last step of basic skin care every morning. Take an adequate amount with the pipette, apply on skin, and gently pat to promote absorption into skin.
* Please review the disclaimer below.
