MISSHA SIGNATURE DRAMATIC WHITENING PACT

Manufacturer
ABLE C&C CO., LTD.
Effective date
2012-10-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:33:23

Label at a glance#

ProductMISSHA SIGNATURE DRAMATIC WHITENING PACT NO.2 SPF50 PLUS PA PLUS PLUS PLUS
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
Label structure8 sections

Indications and uses

INDICATION AND USAGE: After using foundation or BB cream, take an appropriate amount with encased puff and apply it evenly and lightly on face.

Dosage and administration

DOSAGE AND ADMINISTRATION: Use appropriate amount according to your skin condition and apply as you desire. Remove it before sleeping.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS:
Titanium Dioxide 16.71%, Ethylhexyl Methoxycinnamate 6.00%, Zinc Oxide 2.94%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS:
Mica, Talc, Silica, Dimethicone/Vinyl Dimethicone Crosspolymer, Nylon-12, Boron Nitride, Dimethicone, Methicone, Methyl Methacrylate Crosspolymer, Lauroyl Lysine, Phenyl Trimethicone, Pentaerythrityl Tetraisostearate, Iron Oxides, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Triethoxycaprylylsilane, Ethylhexylglycerin, Glyceryl Caprylate, Aluminum Hydroxide, Glycyrrhiza Glabra (Licorice) Root Extract, Hydroxypropyl Bispalmitamide MEA, Ultramarines (CI 77007), Water, Fragrance(Parfum), Zea Mays (Corn) Starch, Hydroxyapatite, Saccharomyces Lysate Extract, Phenoxyethanol, Butylene Glycol, Sodium Hyaluronate, Betula Platyphylla Japonica Juice, Nelumbo Nucifera Flower Water, HDI/Trimethylol Hexyllactone Crosspolymer, Propylene Glycol, Acacia Senegal Gum, Tin Oxide, Dipropylene Glycol, Rosmarinus Officinalis (Rosemary) Extract, Sodium Palmitoyl Proline, Lavandula Angustifolia (Lavender) Extract, Thymus Vulgaris (Thyme) Extract, Origanum Vulgare Leaf/Flower/Stem Extract, Hydrolyzed Rhizobian Gum, Camellia Sinensis Leaf Extract, Vaccinium Macrocarpon (Cranberry) Fruit Extract, Melissa Officinalis Leaf Extract, Rosa Canina Fruit Extract, Aspalathus Linearis Extract, Vaccinium Angustifolium (Blueberry) Fruit Extract, Nymphaea Alba Flower Extract, Hibiscus Sabdariffa Flower Extract, Euterpe Oleracea Fruit Extract, Sigesbeckia Orientalis Extract, Alchemilla Vulgaris Leaf Extract, Rabdosia Rubescens Extract, Hydrolyzed Myrtus Communis Leaf Extract, Hydrogenated Lecithin, Lilium Candidum Flower Extract, Iris Versicolor Extract, Leontopodium Alpinum Flower/Leaf Extract, Nelumbo Nucifera Flower Extract, Rose Extract, Jasminum Officinale (Jasmine) Flower/Leaf Extract, Freesia Refracta Extract, Narcissus Pseudo-Narcissus (Daffodil) Flower Extract, Sophora Angustifolia Root Extract, Saururus Chinensis Leaf/Root Extract, Poncirus Trifoliata Fruit Extract, Caprylyl Glycol, Acanthopanax Senticosus (Eleuthero) Root Extract, Diospyros Kaki Leaf Extract, Viscum Album (Mistletoe) Extract, Oenothera Biennis (Evening Primrose) Flower Extract, Angelica Gigas Root Extract, Adenophora Stricta Root Extract, Zizyphus Jujuba Fruit Extract, Codonopsis Lanceolata Root Extract, Eucommia Ulmoides Extract, Polygonum Odoratum Extract, Sorbus Commixta Extract, Portulaca Oleracea Extract, Oenanthe Javanica Extract, Morus Bombycis Leaf Extract, Cornus Officinalis Fruit Extract, Cuscuta Japonica Seed Extract, Cirsium (Thistle) Flower/Leaf/Stem Extract, Schizandra Chinensis Fruit Extract, Leonurus Sibiricus Flower/Leaf/Stem Extract, Crataegus Cuneata Fruit Extract, Xanthium Strumarium Fruit Extract, Pueraria Thunbergiana Root Extract, Polygonum Multiflorum Root Extract, Eclipta Prostrata Extract, Astragalus Membranaceus Root Extract, Rubus Coreanus Fruit Extract, Saururus Chinensis Extract, Taraxacum Platycarpum Extract, Hydrolyzed Codonopsis Pilosula Root Extract, Aralia Elata Branch/Leaf Extract, Kalopanax Pictus Extract, Lactuca Indica Extract, Cinnamomum Cassia Bark Extract, Glycerin, Caprylhydroxamic Acid

PURPOSE

OTC - PURPOSE SECTION

PURPOSE:
This combination of Cosmetic / OTC Drug can be used as for sun protection and as a cosmetic to cover your blemishes, scar and to tone up your skin care.

WARNINGS

WARNINGS SECTION

WARNING:
For external use only.
Do not swallow.
Keep out of reach of children.
Avoid contact with eyes.
Do not use on exposed wounds or if you are allergic to any ingredients of this product

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

INDICATION AND USAGE:
After using foundation or BB cream, take an appropriate amount with encased puff and apply it evenly and lightly on face.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

DOSAGE AND ADMINISTRATION:
Use appropriate amount according to your skin condition and apply as you desire.
Remove it before sleeping.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138806150631833GTIN-13: 8806150631833
EAN-13: 8806150631833
GTIN storage (14 digits): 08806150631833
missha signature dramatic whitening pact carton.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
13733-015-012019-11-27C16284748780-19855d018-e771-cd31-e053-dbdaa90ab51a849ce669-6691-41eb-9113-5473b982f198

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13733-015-01MISSHA SIGNATURE DRAMATIC WHITENING PACTNO.2 SPF50 PLUS PA PLUS PLUS PLUS11 g in 1 CARTONPOWDER112

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13733-015MISSHA SIGNATURE DRAMATIC WHITENING PACT NO.2 SPF50 PLUS PA PLUS PLUS PLUS (TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE) POWDER [ABLE C&C CO., LTD.]2Legacy NDC, 1 package rows20121025_849ce669-6691-41eb-9113-5473b982f198.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD512
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP2
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z2
OCTINOXATEACTIVE MOIETY4Y5P7MUD512
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP2
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z2
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA2
DimethiconeINACTIVE INGREDIENT92RU3N3Y1O2
Glyceryl CaprylateINACTIVE INGREDIENTTM2TZD4G4A2
WaterINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
13733-01513733-015-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 4 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
Glyceryl CaprylateGLYCERYL MONOCAPRYLATETM2TZD4G4ATABLET / ORAL1 mgExact identifier — unii candidate
2 equally ranked IID candidates
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates
Glyceryl CaprylateGLYCERYL MONOCAPRYLATETM2TZD4G4ACAPSULE / ORAL400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
7074f5d0-8e94-4d19-9f9c-edac53dfa435849ce669-6691-41eb-9113-5473b982f1982012-10-25WarningsExact identifier
spl id: 7074f5d0-8e94-4d19-9f9c-edac53dfa435
spl set id: 849ce669-6691-41eb-9113-5473b982f198

Reported adverse events (FAERS/openFDA)#

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