FDA.reportPublic FDA data

All Aglow Perfect Cushion

Manufacturer
Hankook Cosmetics Manufacturing Co., Ltd._eumseong Factory
Effective date
2016-08-25
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-02 01:24:24

Label at a glance#

ProductAll Aglow Perfect Cushion Foundation
Active ingredientOCTOCRYLENE, ZINC OXIDE, OCTISALATE, OCTINOXATE, TITANIUM DIOXIDE
Label structure9 sections

Dosage and administration

Apply liberally 15 minutes before sun exposure. Reapply at least every 2 hours.

Storage and handling

Protect the product in this container from excessive heat and sun.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 9%

Octyl methoxycinnamate 7%

Octyl Salicylate 4.8%

Octocrylene 2%

Zinc Oxide 2%

INDICATIONS & USAGE SECTION

USES

Helps prevent sunburn.
If used as directed with other sun protection measures - See
Directions- decreases the risk of skin cancer and early skin aging
caused by the sun.

Warnings

WARNINGS SECTION


WARNINGS


– For External use only.
– Keep out of eyes. Rinse with water to remove.
– Stop use if a rash develops. Consult a physician.
.

Directions

DOSAGE & ADMINISTRATION SECTION


Apply liberally 15 minutes before sun exposure.
Reapply at least every 2 hours.

Other information

STORAGE AND HANDLING SECTION

  • Protect the product in this container from excessive heat and sun.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, CYCLOPENTASILOXANE (CYCLOMETHICONE), DIPHENYLSILOXY
PHENYL TRIMETHICONE, CYCLOHEXASILOXANE (CYCLOMETHICONE),
C12-15 ALKYL BENZOATE, NIACINAMIDE, CAPRYLYL METHICONE,
TRIMETHYLSILOXYSILICATE, PEG-30 DIPOLYHYDROXYSTEARATE,
PEG-10 DIMETHICONE, BUTYLENE GLYCOL, VINYL
DIMETHICONE/METHICONE SILSESQUIOXANE CRTOSSPOLYMER,
SODIUM CHLORIDE, QUATERNIUM-18 BENTONITE,
ACRYLATES/STEARYL ACRYLATE/DIMETHICONE METHACRYLATE
COPOLYMER, POLYMETHYL METHACRYLATE, IRON OXIDE,
DIMETHICONE, ACRYLATES/DIMETHICONE COPOLYMER, BORON
NITRIDE, CHLORPHENESIN, TRIETHOXYCAPRYLYLSILANE,
ALUMINA (CI 77002), CITRUS MEDICA LIMONUM (LEMON) PEEL
OIL, ADENOSINE, HONEY, LAVANDULA ANGUSTIFOLIA (LAVENDER)
OIL, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL,
EUCALYPTUS GLOBULUS LEAF OIL, CITRUS AURANTIUM DULCIS
(ORANGE) PEEL OIL, CITRUS GRANDIS (GRAPEFRUIT) PEEL OIL,
HYDROGENATED LECITHIN, 1,2-HEXANEDIOL, CHOLESTEROL,
PEG-800, GLYCERIN, POLYSORBATE 20, SH-OLIGOPEPTIDE-1,
SH-POLYPEPTIDE-1, SH-POLYPEPTIDE-8, SH-POLYPEPTIDE-9,
SH-POLYPEPTIDE-45, SH-OLIGOPEPTIDE-2, SH-POLYPEPTIDE-22.

OTC - PURPOSE SECTION

PURPOSE

SUNSCREEN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

If product is swallowed, get medical help or contact a poison control center right away

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58544-001-012024-11-01C16284748780-19d75b9d0-cf82-f424-e053-dadaa90a57ce3aeb55c7-2907-6dd7-e054-00144ff8d46c
58544-001-012020-01-31C16284748780-19d75b9d0-cf82-f424-e053-dadaa90a57ce3aeb55c7-2907-6dd7-e054-00144ff8d46c

Products#

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

DailyMed product names page 1 of 2 · 46 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58544-00158544-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 44 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTOCRYLENE5A68WGF6WMACTIB
ZINC OXIDESOI2LOH54ZACTIB
GLYCERINPDC6A3C0OXIACT
POLYSORBATE 207T1F30V5YHIACT
PEG-80 STEARATE1X2OAT3BFKIACT
EUCALYPTUS OIL2R04ONI662IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
DIPHENYLSILOXY PHENYL TRIMETHICONEI445L28B12IACT
CITRUS MEDICA FRUITZE5Q6PN9ONIACT
ALUMINUM HYDROXIDE SULFATE (AL(OH)(SO4))9QO62ZS7VOIACT
CYCLOMETHICONE 6XHK3U310BAIACT
HYDROGENATED SOYBEAN LECITHINH1109Z9J4NIACT
CYCLOMETHICONE 50THT5PCI0RIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
NIACINAMIDE25X51I8RD4IACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8)5041RX63GNIACT
PEG-30 DIPOLYHYDROXYSTEARATE9713Q0S7FOIACT
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
SODIUM CHLORIDE451W47IQ8XIACT
BENTOQUATAM7F465U79Q1IACT
STEARYL CAPRYLATE06TS6O9194IACT
POLY(METHYL METHACRYLATE; 450000 MW)Z47NNT4J11IACT
BROWN IRON OXIDE1N032N7MFOIACT
DIMETHICONE92RU3N3Y1OIACT
BORON NITRIDE2U4T60A6YDIACT
CHLORPHENESINI670DAL4SZIACT
CAPRYLYL GLYCOL00YIU5438UIACT
TRIETHOXYCAPRYLYLSILANELDC331P08EIACT
OCTISALATE4X49Y0596WACTIB
OCTINOXATE4Y5P7MUD51ACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
CHOLESTEROL97C5T2UQ7JIACT
CITRUS MAXIMA FRUIT RIND OIL8U3877WD44IACT
ORANGE OILAKN3KSD11BIACT
ROSEMARY OIL8LGU7VM393IACT
LAVENDER OILZBP1YXW0H8IACT
HONEYY9H1V576FHIACT
JUNIPERUS DEPPEANA WOOD OIL4739QA5686IACT

Source Document#

Source XML · Source PDF

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
25d44f7f-6f8c-cca2-e063-6294a90a330f3aeb55c7-2907-6dd7-e054-00144ff8d46c2024-11-01WarningsExact identifier
spl set id: 3aeb55c7-2907-6dd7-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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