FDA.reportPublic FDA data

M Suit Cushion

Manufacturer
Cnt Dream. Co., Ltd
Effective date
2020-10-26
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 23:09:51

Label at a glance#

ProductM Suit Cushion
Active ingredientZINC OXIDE, TITANIUM DIOXIDE, OCTINOXATE, OCTISALATE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

OTC - ACTIVE INGREDIENT SECTIONOTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide, Ethylhexyl Methoxycinnamate, Zinc Oxide, Ethylhexyl Salicylate

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT SECTIONINACTIVE INGREDIENT SECTION

Chamaecyparis Obtusa Leaf Extract,Cyclopentasiloxane,Butylene Glycol,Glycerin,
Cyclohexasiloxane,Sodium Hyaluronate,Caprylic/Capric Triglyceride,Cyclomethicone,
Trimethylsiloxysilicate,Arbutin,1,2-Hexanediol,Cetyl PEG/PPG-10/1 Dimethicone,
Iron Oxide Yellow(CI 77492),PEG-10 Dimethicone,Sodium Chloride,Sorbitan Sesquioleate,
Iron Oxide Red (CI 77491),Methicone,Triethoxycaprylylsilane,Lavandula Angustifolia
(Lavender) Extract,Rosmarinus Officinalis (Rosemary) Extract,Origanum Vulgare
Flower/Leaf/Stem Extract,Thymus Vulgaris (Thyme) Extract,Vaccinium Angustifolium
(Blueberry) Fruit Extract,Fragrance, Iron Oxide Black (CI77499),Ethylhexylglycerin,
Adenosine

OTC - ASK DOCTOR SECTION

OTC - ASK DOCTOR SECTIONOTC - ASK DOCTOR SECTION

*Stop use and ask a doctor if rash or irritation develops and lasts.

OTC - DO NOT USE SECTION

OTC - DO NOT USE SECTIONOTC - DO NOT USE SECTION

*Do not use on damaged or broken skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

OTC - KEEP OUT OF REACH OF CHILDREN SECTIONOTC - KEEP OUT OF REACH OF CHILDREN SECTION

*Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

WARNING SECTION

WARNINGS SECTION

WARNING SECTIONWARNING SECTION

*For external use only
*Do not use on damaged or broken skin
*When using this product keep out of eyes, Rinse with water to remove.
*Stop use and ask a doctor if rash or irritation develops and lasts.
*Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

OTC - PURPOSE

OTC - PURPOSE SECTION

OTC - PURPOSEOTC - PURPOSE

Sunscreen

INDICATIONS & USAGE SECTION

INDICATIONS & USAGE SECTIONINDICATIONS & 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

Directions:
Apply a proper amount evenly for the last step of skin care.
For sunscreen use:
*apply liberally 15 minutes before sun exposure
*reapply at least every 2 hours
*use a water resistant sunscreen if swimming or sweating
*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 10a.m-2p.m
*wear long-sleeved shirts, pants, hats, and sunglasses
*children under 6 months of age: Ask a doctor

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL. PRINCIPAL DISPLAY PANELPACKAGE LABEL. PRINCIPAL DISPLAY PANEL

M Suit Cushion

SPF50+ PA+++

UV Protection

Net Wt. 21g/0.740Oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71909-1237-12024-01-16C16284748780-1d6a99b39-979e-a426-e053-dadaa90af4c2M Suit Cushion SPF50+ PA+++
71909-1237-12022-01-28C16284748780-1d6a99b39-979e-a426-e053-dadaa90af4c2M Suit Cushion SPF50+ PA+++

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71909-123771909-1237-0, 71909-1237-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM CHLORIDE451W47IQ8XIACT
ZINC OXIDESOI2LOH54ZACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
CHAMAECYPARIS OBTUSA LEAF7OL154J5XBIACT

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
0f1b5098-2b6b-aa31-e063-6394a90adf865fcb023f-e11a-7483-e053-2991aa0a47452024-01-16WarningsExact identifier
spl set id: 5fcb023f-e11a-7483-e053-2991aa0a4745

Reported adverse events (FAERS/openFDA)#

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