PurpleU GLOW BEAUTIFULLY BRIGHT

Manufacturer
Purple U Co., Ltd | RECIPE CO., LTD
Effective date
2020-09-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:22

Label at a glance#

ProductPurpleU GLOW BEAUTIFULLY BRIGHT
Active ingredientDIMETHICONE, TITANIUM DIOXIDE, ZINC OXIDE, NIACINAMIDE, ADENOSINE
Label structure10 sections

Indications and 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

Dosage and administration

Apply liberally 15 minutes before sun exposure Reapply at least every 2 hours Use 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 sun, especially from 1...

Storage and handling

Protect this product from excessive heat and direct sun

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Dimethicone 1.0%

Titanium Dioxide 5.89%

Zinc Oxide 4.90%

Niacinamide 2.0%

Adenosine 0.04%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Sunscreen

Brightening

Wrinkle improvement

Uses

DOSAGE & ADMINISTRATION SECTION

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

Warnings

WARNINGS 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

OTC - ASK DOCTOR SECTION

rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Poison Control Center right away.

Directions

INDICATIONS & USAGE SECTION

  • Apply liberally 15 minutes before sun exposure
  • Reapply at least every 2 hours
  • Use 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 sun, especially from 10a.m.–2 p.m.
  • Wear long-sleeved shirts, pants, hats, and sunglasses
  • Children under 6 months: ask a doctor

Other information

STORAGE AND HANDLING SECTION

Protect this product from excessive heat and direct sun

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Water, Dimethicone, Cyclohexasiloxane, Titanium Dioxide (CI 77891), Ethylhexyl Methoxycinnamate, Zinc Oxide (CI 77947), Dimethicone Crosspolymer, Cetyl PEG/PPG-10/1 Dimethicone, Isotridecyl Isononanoate, Glycerin, Niacinamide, Dicaprylyl Carbonate, HDI/Trimethylol Hexyllactone Crosspolymer, Hydrogenated Poly(C6-14 Olefin), Lauryl PEG-10 Tris(Trimethylsiloxy)silylethyl Dimethicone, Pentylene Glycol, Polymethyl Methacrylate, Citrus Aurantium Dulcis (Orange) Peel Oil, Boswellia Carterii Oil, Pelargonium Graveolens Flower Oil, Vetiveria Zizanoides Root Oil, Amyris Balsamifera Bark Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Daucus Carota Sativa (Carrot) Seed Oil, Adansonia Digitata Seed Oil, Argania Spinosa Kernel Oil, Hydrolyzed Hyaluronic Acid, Olea Europaea (Olive) Fruit Oil, Hydrolyzed Collagen, Rose Flower Oil, Adansonia Digitata Fruit Extract, PEG-10 Dimethicone, Silica, Disteardimonium Hectorite, Magnesium Sulfate, Synthetic Fluorphlogopite, Stearic Acid, Triethoxycaprylylsilane, Ethylhexylglycerin, Adenosine, Butylene Glycol, Dipalmitoyl Hydroxyproline, Sodium Cocoyl Alaninate, Tocopherol, Disodium EDTA, Phenoxyethanol, Fragrance(Parfum), Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499)

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

35ml NDC: 90069-202-01 Label35ml NDC: 90069-202-01 Label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
90069-202-012022-07-01C16284748780-1d6a99b39-466a-a426-e053-dadaa90af4c290069-202
90069-202-012022-01-28C16284748780-1d6a99b39-466a-a426-e053-dadaa90af4c290069-202

Products#

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

DailyMed product names page 1 of 2 · 45 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90069-20290069-202-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 43 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
e17460cd-733e-5944-e053-2a95a90a2f75ae53a49b-7c1e-38c0-e053-2995a90a0a272022-06-14WarningsExact identifier
spl set id: ae53a49b-7c1e-38c0-e053-2995a90a0a27

Reported adverse events (FAERS/openFDA)#

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