Sun Project Shimmer Sun Essence

Manufacturer
THANK YOU FARMER CO., LTD. | Kolmar Korea Co.,LTD. Gwanjeong Factory
Effective date
2021-08-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:38:24

Label at a glance#

ProductSun Project Shimmer Sun Essence
Active ingredientOCTINOXATE, OCTISALATE, TITANIUM DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethylhexyl Methoxycinnamate 6.00%
Ethylhexyl Salicylate 3.00%
Titanium Dioxide 1.22%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Helps prevent sunburn

DOSAGE & ADMINISTRATION SECTION

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


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 of 15 of higher and other sun protection measures including: 1) Limited time in the sun, especially from 10 am to 2 pm. 2) Wear long-sleeve shirts, pants, hats, and sunglasses

Ask a doctor to use for children under 6 months

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

Stop using and ask a doctor if rash occurs

When using this product, keep out of eyes. Rinse with water to remove

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

INACTIVE INGREDIENT SECTION

Water, Cyclopentasiloxane, Glycerin, Alcohol, Caprylic/Capric Triglyceride, Isoamyl P-Methoxycinnamate, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Niacinamide, Glyceryl Stearate, Butyrospermum Parkii (Shea) Butter, Dimethicone, Polysorbate 60, Mica, 1,2-Hexanediol, Silica, Peg-100 Stearate, Cetearyl Alcohol, Triethoxycaprylylsilane, Portulaca Oleracea Extract, Phenoxyethanol, Beeswax, Ammonium Acryloyldimethyltaurate/Vp Copolymer, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Stearic Acid, Fragrance, Tocopheryl Acetate, Sodium Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyurethane-11, Xanthan Gum, Isohexadecane, Polysorbate 80, Adenosine, Disodium Edta, Tin Oxide, Red 4 (Ci 14700), Nelumbo Nucifera Flower Water, Plukenetia Volubilis Seed Oil, Aloe Barbadensis Leaf Extract, Althaea Rosea Flower Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70618-004-022024-03-26C16284748780-11030e365-155e-111a-e063-dadaa90a10e270618-004 Sun Project Shimmer Sun Essence
70618-004-022024-01-30C16284748780-11030e365-155e-111a-e063-dadaa90a10e270618-004 Sun Project Shimmer Sun Essence

Products#

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

DailyMed product names page 1 of 2 · 42 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70618-00470618-004-01, 70618-004-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 40 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
149a457f-1f69-95ae-e063-6294a90a8fc79da7451a-7c45-49f9-b4e9-84971bb16f1f2024-03-26WarningsExact identifier
spl set id: 9da7451a-7c45-49f9-b4e9-84971bb16f1f

Reported adverse events (FAERS/openFDA)#

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