Microfit Cushion 101

Manufacturer
Codecosme International Co., Ltd. | Cosmecca Korea Co., Ltd.
Effective date
2017-10-18
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:43

Label at a glance#

ProductMicrofit Cushion 101
Active ingredientTitanium Dioxide, Octinoxate, Octisalate
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Titanium Dioxide 9.66%, Ethylhexyl Methoxycinnamate 6.70%, Ethylhexyl Salicylate 4.00%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Bambusa Vulgaris Water, Cyclopentasiloxane, Trimethylsiloxysilicate, Butylene Glycol Dicaprylate/Dicaprate, PEG-8 Dimethicone, Methyl Methacrylate Crosspolymer, Pentylene Glycol, Butylene Glycol, Glycerin, Niacinamide, Mica (CI 77019), Dimethicone, Silica, Cetyl PEG/PPG-10/1 Dimethicone, Dipropylene Glycol, Magnesium Sulfate, Phenoxyethanol, Iron Oxides (CI 77492), Caprylyl Methicone, Dimethicone/Vinyl Dimethicone Crosspolymer, Diphenyl Dimethicone, Fragrance(Parfum), Water, Stearic Acid, Alumina, Disteardimonium Hectorite, Iron Oxides (CI 77491), Triethoxycaprylylsilane, Aluminum Hydroxide, Ethylhexylglycerin, Iron Oxides (CI 77499), Adenosine, Disodium EDTA, Calcium Carbonate, Polymethylsilsesquioxane, Gossypium Herbaceum (Cotton) Powder, Caprylic/Capric Triglyceride, Lecithin, Polyglutamic Acid, Cassia Angustifolia Seed Polysaccharide, Phospholipids, Ceramide NP, 1,2-Hexanediol, Cholesterol, Arginine, Phytosterols

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings: 1. If any of the following symptoms occur when using the product, stop using immediately and consult a dermatologist. a) red spots, swelling, itchy rashes other skin irritations, etc. b) if a) occurs after applying and being exposed to sunlight. 2. Do not use on wounds, inflamed skin, itchy areas, or other infected areas. 3. Storage and handling: a) must close cap after use. b) Keep out of reach of children. c) keep away from extreme heat, cold and direct sunlight. d) Avoid contact with eyes. In case of contact with eyes, rinse thoroughly with water. 4. For external use only.

DESCRIPTION

DESCRIPTION SECTION

Uses: An ultra-light and non-oxidizing cushion foundation that allows layering without caking. Perfect for mid-day touch ups.

Directions: 1. Gently soak the applicator puff on to mesh to use product. 2. Start from inner areas of the face and work outwards 3. Softly swipe over the skin to spread evenly before applying the foundation. * Coverage can build up by layering a small amount several times. 4. Close cap after use. 5. To refill the product: Open outer cap, but close the inner cap and flip over the product. While holding the product push down on the bottom sticker with both thumbs while having outer cap open. Once the existing container is removed, replace it with a refill with the hinge set on the dipped area which is on the left hand side.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71786-020-022020-01-31C16284748780-19d75b9d0-e455-f424-e053-dadaa90a57ce472ef14d-b4f3-4881-b7d3-34597d01107c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71786-020-01Microfit Cushion 10112 g in 1 CONTAINERPOWDER121
71786-020-02Microfit Cushion 1011 in 1 CARTONPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71786-020MICROFIT CUSHION 101 (TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE) POWDER [CODECOSME INTERNATIONAL CO., LTD.]1Legacy NDC, 2 package rows20171018_472ef14d-b4f3-4881-b7d3-34597d01107c.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71786-02071786-020-01, 71786-020-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
c7838c80-4aee-49c6-a2bc-e9ad3b3bfac0472ef14d-b4f3-4881-b7d3-34597d01107c2017-10-18WarningsExact identifier
spl id: c7838c80-4aee-49c6-a2bc-e9ad3b3bfac0
spl set id: 472ef14d-b4f3-4881-b7d3-34597d01107c

Reported adverse events (FAERS/openFDA)#

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