DAL INNER CUSHION

Manufacturer
E&B | EYESOME. Co.,Ltd.
Effective date
2020-03-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:38:24

Label at a glance#

ProductDAL INNER CUSHION
Active ingredientTitanium Dioxide, Octinoxate, Zinc Oxide
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: 

Titanium Dioxide 7.6%
Ethylhexyl Methoxycinnamate 7.0%
Zinc Oxide 0.98%

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:

1)After or while using the cosmetic product, if redness, swelling, itchiness, or any other similar symptom or discomfort arises upon contact with direct sunline, please consult a healthcare provider before using any further
2)Avoid using on wounded areas
3)Important notes for storage and handling
a) Store at places where children cannot reach
b) Store at places with no direct sunlight
4)Avoid contact with eye

DESCRIPTION

DESCRIPTION SECTION

Uses:
Whitening Anti-wrinkle UV protection triple function

Directions:
Use the built-in DAL inner puff to apply and pat gently

Questions:
+8215224401

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

Water, Cyclopentasiloxane, Butylene Glycol, Phenyl Trimethicone, Cyclohexasiloxane, Butylene Glycol Dicaprylate/Dicaprate, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Methylene Bis-Benzotriazolyl Tetramethylbutylphenol, Methylpropanediol, Niacinamide, Synthetic Fluorphlogopite, Hydrogenated C6-14 Olefin Polymer, Polypropylsilsesquioxane, Sodium Chloride, Dimethicone, Acrylates/Stearyl Acrylate/Dimethicone Methacrylate Copolymer, Aloe Barbadensis Leaf Juice, Biosaccharide Gum-1, Sorbitan Isostearate, Vegetable Oil, Polyhydroxystearic Acid, Acrylates/Ethylhexyl Acrylate/Dimethicone Methacrylate Copolymer, Beeswax, Decyl Glucoside, Disteardimonium Hectorite, Phenoxyethanol, Dimethicone/PEG-10/15 Crosspolymer, Aluminum Hydroxide, Caprylyl Glycol, Triethoxycaprylylsilane, Ethylhexyl Palmitate, Isopropyl Myristate, Isostearic Acid, Lecithin, Methyl Methacrylate Crosspolymer, Xanthan Gum, Propanediol, Tocopheryl Acetate, HDI/Trimethylol Hexyllactone Crosspolymer, Polyglyceryl-3 Polyricinoleate, Caprylhydroxamic Acid, Glycerin, Adenosine, Disodium EDTA, Acrylates/Tridecyl Acrylate/Triethoxysilylpropyl Methacrylate/DimethiconeMethacrylate Copolymer, Propylene Glycol, Dipropylene Glycol, Silica, Sodium Citrate, Bacillus/Soybean Ferment Extract, Tocopherol, 1,2-Hexanediol, Pentylene Glycol, Alteromonas Ferment Extract, Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499), Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73759-03073759-030-01, 73759-030-02

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

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c4795db4-21ef-5600-e053-2995a90a2ed2500f5d28-df93-43b9-bc79-d04af8e213de2021-06-11WarningsExact identifier
spl set id: 500f5d28-df93-43b9-bc79-d04af8e213de

Reported adverse events (FAERS/openFDA)#

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