67225-5333 AGE20S SUNSCREEN DUO

Manufacturer
Aekyung Industrial Co., Ltd.
Effective date
2026-04-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:52:59

Label at a glance#

ProductAGE20S SUNSCREEN DUO
Active ingredientZINC OXIDE, AVOBENZONE, OCTOCRYLENE, OCTISALATE, HOMOSALATE
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


AGE20S UV DEFENSE HYDRO CALMING SUNSCREEN

Avobenzone 2.70%
Homosalate 7.00%
Octisalate 4.50%
Octocrylene 9.00%

AGE20S UV MINERAL PRIMING SUNSCREEN
Zinc Oxide 14.68%

OTC - PURPOSE SECTION

Sunscree

INDICATIONS & USAGE SECTION

■ Helps prevent sunburn.
■ If used as directed with other sun protection measures (see Driections), decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

■ on damaged or broken skin.

OTC - WHEN USING SECTION

■ keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

Stop use and ask a doctor if ■ rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact poison control center right away.

DOSAGE & ADMINISTRATION SECTION

■ apply liberally 15 minutes before sun exposure.
■ children under 6 months of age: Ask a doctor.
■ Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
■ limit time in the sun, especially from 10 a.m-2 p.m
■ wear long-sleeved shirts, pants, hats, and sunglasses
■ reapply at least every 2 hours.
■ use a water resistant sunscreen if swimming or sweating

OTHER SAFETY INFORMATION

■ Protect the product in the container from excessive heat and avoid storing it under direct sun.

INACTIVE INGREDIENT SECTION

AGE20S UV DEFENSE HYDRO CALMING SUNSCREEN
Water, Propanediol, Butyloctyl Salicylate, Polyglyceryl-3 Distearate, Silica, Microcrystalline Cellulose, C13-15 Alkane, Panthenol, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extr Hydroxyhydrocinnamate, Benzotriazolyl Dodecyl p-Cresol, Hydroxyacetophenone, Sodium Stearoyl Glutamate, Butylene Glycol, Allantoin, Ammonium Polyacryloyldimethyl Taurate, Cetear Oleic Acid, Caprylhydroxamic Acid, Ethanol, Cellulose Gum, 1,2-Hexanediol, Oryza Sativa (Rice) Bran Extract, Scutellaria Baicalenesis Root Extract, Tris(Tetramethylhy- droxypiperidinol) Hyaluronic Acid, Ceramide NP

AGE20S UV MINERAL PRIMING SUNSCREEN
Water, Dimethicone ,Butyloctyl Salicylate, Propanediol, Ethylhexyl Methoxycrylene, PEG-10 Dimethicone, Phenyl Trimethicone, Silica, Zeolite, Caprylyl Methicone, Glyceryl Glucoside, Lauryl PEG-10 Tris(Trimethylsiloxy)silylethyl Dimethicone, Glycerin, Magnesium Sulfate, Dimethicone/Vinyl Dimethicone Crosspolymer, Panthenol, Calcium Aluminum Borosilicate, Aloe Barbadensis Leaf Extract, Dipropylene Glycol, Benzotriazolyl Dodecyl p-Cresol, Pentaerythrityl Tetra-di-t-butyl Hydroxyhydrocinnamate, Triethoxycaprylylsilane, C30-45 Alkyl Cetearyl Dimethicone Crosspolymer, Disteardimonium Hectorite, Hydroxyacetophenone
Allantoin, Caprylyl Glycol, Caprylhydroxamic Acid, Titanium Dioxide, Butylene Glycol, Tin Oxide, 1,2-Hexanediol, Dibutyl Adipate
Neopentyl Glycol Diheptanoate, C15-23 Alkane, Hydrogenated Lecithin, Cetearyl Alcohol, Stearic Acid, C13-14 Alkane, Bakuchiol
Camellia Sinensis Leaf Extract, Hyaluronic Acid, Pentasodium Tetracarboxymethyl Heptadecanoyl Dipeptide-12, Tocopherol, Ceramide NP, Ceramide NS, Cholesterol, Phytosphingosine, Ceramide AP, Ceramide AS, Ceramide EOP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sunscreen_PR_Outbox_1Sunscreen_PR_Outbox_1Sunscreen_PR_Outbox_2Sunscreen_PR_Outbox_2Sunscreen_PRSunscreen_PR

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67225-5033-1AGE20S SUNSCREEN DUO50 g in 1 TUBECREAM50 g4.5 g in 50g1
67225-5033-2AGE20S SUNSCREEN DUO1 in 1 BOXCREAM4.5 g in 50g1
67225-5301-4AGE20S SUNSCREEN DUO50 g in 1 TUBECREAM50 g7.34 g in 50g1
67225-5301-5AGE20S SUNSCREEN DUO1 in 1 BOXCREAM7.34 g in 50g1
67225-5333-1AGE20S SUNSCREEN DUO1 in 1 CARTONKIT11

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 2 · 78 matching rows.

NDC Codes#

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 3 · 92 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 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AGE20S UV MINERAL PRIMING SUNSCREENZINC OXIDEAekyung Industrial Co., Ltd.43c1f70b-0664-40be-e063-6394a90a2b482026-04-08WarningsExact identifier
ndc (package): 67225-5301-5
ndc (package): 67225-5301-4
ndc (product): 67225-5301
ndc11 (package): 67225530105
ndc11 (package): 67225530104
AGE20S SUNSCREEN DUOZINC OXIDE, AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENEAekyung Industrial Co., Ltd.4eef11cd-85a1-0e44-e063-6394a90a5d442026-04-08WarningsExact identifier
ndc (package): 67225-5301-5
ndc (package): 67225-5333-1
ndc (package): 67225-5301-4
ndc (package): 67225-5033-1
ndc (package): 67225-5033-2
ndc (product): 67225-5333
ndc11 (package): 67225503302
ndc11 (package): 67225530105
ndc11 (package): 67225533301
ndc11 (package): 67225530104
ndc11 (package): 67225503301
spl id: 4eef170d-8ffc-0fc1-e063-6394a90a908c
spl set id: 4eef11cd-85a1-0e44-e063-6394a90a5d44
AGE20S UV DEFENSE HYDRO CALMING SUNSCREENOCTOCRYLENE, HOMOSALATE, OCTISALATE, AVOBENZONEAekyung Industrial Co., Ltd.1e9a5c77-7027-3b52-e063-6394a90ac0eb2025-12-09WarningsExact identifier
ndc (package): 67225-5033-1
ndc (package): 67225-5033-2
ndc (product): 67225-5033
ndc11 (package): 67225503302
ndc11 (package): 67225503301

Reported adverse events (FAERS/openFDA)#

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