Age 20s ESSENCE COVER PACT ORIGINAL WHITE LATTE 13

Manufacturer
Aekyung Industrial Co., Ltd. | Aekyung Ind. Co., Ltd._Chungyang Factory
Effective date
2017-06-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:15:57

Label at a glance#

ProductAge 20s ESSENCE COVER PACT ORIGINAL WHITE LATTE 13
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OCTOCRYLENE
Label structure10 sections

Storage and handling

- Avoid high/low temperatures and direct sunlight when storing - Protect the product in the container from excessive heat and direct sun

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Titanium dioxide (8.86%), Ethylhexyl Methoxycinnamate (7%), Octocrylene (4%), Diethylamino Hydroxybenzoyl Hexyl Benzoate (3%)

OTC - PURPOSE SECTION

Purpose Skin Protectant

INDICATIONS & USAGE SECTION

Uses: Helps prevent sunburn

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

OTC - WHEN USING SECTION

Use the product as directed.  Always close the cap after use.  Please do not crush or drop the products.  Please handle with care.

OTC - DO NOT USE SECTION

- Do not use the product if you experience the following symptoms.  May lead to worsening symptoms if you continue to use the product so please consult a dermatologist

  - If you experience red spots, swelling, itchiness or irritation

  - If you experience the symptoms above when exposed to direct sunlight

- Do not use on damaged skin or when suffering from eczema or dermatitis

- Do not consume.  Consult your physician immediately if swallowed

INSTRUCTIONS FOR USE SECTION

Apply the product on your skin with the included applicator by rubbing the product with the applicator and gently patting it on skin.  If in eyes, rinse immediately with running water.

STORAGE AND HANDLING SECTION

- Avoid high/low temperatures and direct sunlight when storing
- Protect the product in the container from excessive heat and direct sun

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Hyaluronic Acid, Hydrolyzed Hyaluronic Acid, Sodium Hyaluronate, Phenyl Trimethicone, Cyclopentasiloxane, Niacinamide, Euphorbia Cerifera (Candella) Wax, Dimethicone, Cyclohexasiloxane, Hydrogenated Polyisobulene, CI 77492, Silica, Cetyl PEG/PPG-10/1 Dimethicone, Sodium Glutamate, VP/Hexadecene Copolymer, Aluminum Hydroxide, C30-45 Alkyl Methicone, p-Anisic Acid, Stearic Acid, Dimethicone PEG-10/15 Crosspolymer, C30-45 Olefin, Glyceryl Caprylate, CI 77491, Triethoxycaprylylsilane, Alumina, Butylene Glycol, Perfume, Synthetic Sapphire, CI 77499, Dipropylene Glycol, Cetearyl Nonanoate, Adenosine, Lavandula Angustifolia (Lavender) Extract, Origanum Vulgare Flower/Leaf/Stem Extract, Polymethylsilsesquioxane, Rosmarinus Officinalis (Rosemary) Extract, Thymus Vulgaris (Thyme) Extract, Water, Citrus Medica Limonum (Lemon) Fruit Extract, milk protein extract, Pearl Powder, Saussurea Involucrata Extract, Terminalia Ferdinandiana Fruit Extract, Yeast Ferment Extract, Aspergillus/Camellia Sinensis Leaf Extract Ferment Filtrate, Aureobasidium Pullalans Ferment Filtrate, Bifida Ferment Filtrate, Galactomyces Ferment Filtrate, Lactobacillus/Collagen Ferment Filtrate, Lactobacillus/Purica Granatum Fruit Juice Ferment Filtrate, Lactobacillus/Royal Jelly Ferment Filtrate, Lactobacillus/Soybean Extract Ferment Filtrate, Vitreoscilia Ferment, Glycerin, Madecassoside, Diamond Powder, Ruby Powder, Mica, Pentylene Glycol, 1,2-Hexanediol, Caprylyl Glycol, Hydroxyapatite, Carbomer, Sodium Lactate, Hydrogenated Lecithin, Phenoxyethanol, Polysorbate 20, Zinc Oxide, Palmitoyl Tripeptide-1, rh-Oligopeptide-1, Palmitoyl Tetrapeptide-7

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67225-041367225-0413-1

Ingredients#

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Source Document#

Source XML

openFDA label cross-check#

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
98ba2622-8a4f-68ec-e053-2a95a90aa53cadbd6501-1e8f-42bf-bfc9-fb3f4bab2b6a2019-12-02Exact identifier
spl set id: adbd6501-1e8f-42bf-bfc9-fb3f4bab2b6a

Reported adverse events (FAERS/openFDA)#

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