LovLuv M Suit Sun Block

Manufacturer
Cnt Dream. Co., Ltd
Effective date
2020-10-26
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:09:49

Label at a glance#

ProductLovLuv M Suit Sun Block
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, ZINC OXIDE
Label structure10 sections

Label contents#

Full prescribing information#

OTC - Active Ingredient Section

OTC - Active Ingredient SectionOTC - Active Ingredient Section

Titanium Dioxide, Ethylhexyl Methoxycinnamate, Ethylhexyl Salicylate, Zinc Oxide

Inactive Ingredient Section

Inactive Ingredient SectionInactive Ingredient Section

Chamaecyparis Obtusa Leaf Extract, Cyclopentasiloxane, Butylene Glycol, Silica,
Cyclohexasiloxane, Niacinamide, 1,2-Hexanediol, Cetyl PEG/PPG-10/1 Dimethicone,
Sorbitan Sesquioleate, PEG-10 Dimethicone, Hexyl Laurate, Sodium Chloride, Ozokerite,
Caprylic/Capric Triglyceride, Stearic Acid, Alumina, Xanthan Gum, 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 Yellow(CI 77492), Ethylhexylglycerin,Adenosine, Iron Oxide Red (CI 77491)

OTC-ASK ODCTOR SECTION

OTC - ASK DOCTOR SECTION

OTC-ASK ODCTOR SECTIONOTC-ASK ODCTOR 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

WARNINGS SECTION

WARNINGS SECTIONWARNINGS SECTION

Warnings
*For external use only
*Do not use on damaged or broken skin
*When using this product keep our 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 SECTION

OTC - PURPOSE SECTIONOTC - PURPOSE SECTION

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

Dosage & administration section

Dosage & administration sectionDosage & administration section

M Suit Sun Block SPF50+ PA+++

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PACKAGE LABEL. PRINCIPAL DISPLAY PANELPACKAGE LABEL. PRINCIPAL DISPLAY PANEL

M Suit Sun Block
SPF50+ PA+++

UV Protection

Net WT. 50ml. 1.69 Fl. Oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71909-1220-12024-01-16C16284748780-1d6a99b39-9792-a426-e053-dadaa90af4c2M Suit Sun Block SPF50+ PA+++
71909-1220-12022-01-28C16284748780-1d6a99b39-9792-a426-e053-dadaa90af4c2M Suit Sun Block SPF50+ PA+++

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
71909-122071909-1220-0, 71909-1220-1

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
0f1c2df2-8526-f166-e063-6394a90a4a855f7a9b43-c77f-3822-e053-2a91aa0a042b2024-01-16WarningsExact identifier
spl set id: 5f7a9b43-c77f-3822-e053-2a91aa0a042b

Reported adverse events (FAERS/openFDA)#

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