Hyaluronic acid UV clear sunscreen SPF 55

Manufacturer
Skinidea Co., Ltd. | COSMAX, INC.
Effective date
2024-07-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:53:52

Label at a glance#

ProductHyaluronic acid UV clear sunscreen SPF 55
Active ingredientZINC OXIDE, HOMOSALATE, OCTOCRYLENE, OCTISALATE
Label structure13 sections

Indications and uses

helps prevent sunburn if used as directed withother sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide 10.38%

Homosalate 6%

Octocrylene 5%

Ethylhexyl salicylate 4.5%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • if used as directed withother 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

OTC - DO NOT USE SECTION

  • on damaged or broken skin

When using this product

OTC - WHEN USING SECTION

  • keepout of eyes.  Rinse with water to remove.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rash occurs

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Sun Protection Measures.

DOSAGE & ADMINISTRATION SECTION

  • For sunscreen use:
  • apply liberally 15 minutes before sun exposure
  • use a water resistent sunscreen if swimming or sweating
  • reapply at least every 2 hours

Sun Protection Measures.

Spending time in the sun increases your risk of skin aging.  To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including: 

limit time in the sun, especially from 10 a.m. - 2 p.m. 

wear long-sleeve shirts, pants, hats, and sunglasses

children under 6 months: Ask a doctor.

Inactive Ingredients:

INACTIVE INGREDIENT SECTION

Water, Caprulic/Capric Triglyceride, Propanediol, Glycerin, Coco-Caprylate/Caparte, Cetearyl Olivate, 1,2-Hexanediol, Pentylene Glycol, Sorbitan Olivate, Cetearyl Alcohol, Glyceryl Stearate, Potassium Cetyl Phosphate, Lauroyl Lysine, Polyhydroxystearic Acid, Hydroxyacetophenone, Panthenol, Sodium Polyacryloyldimethyl Taurate, Triethoxycaprylylsilane, Acrylates Copolymer, Stearic Acid, Tromethamine, Sphingomonas Ferment Extract, Neopentyl Glycol Diethylhexanote, Polyacrylate Crosspolymer-6, Hydroxypropyl Methylcellulose Stearoxy Ether, Trisodium Ethylenediamine Disuccinate, Citrullus Lanatus (Watermelon) Fruit Extract, Citric Acid, Acetyl Glucosamine, Sodium Hyaluronate, Biosaccharide Gun-1, Ethylhexylglycerin, Sodium Hyaluronate Crosspolymer, Gluconolactone, Salix Alba (Willow) Bark Extract, Butylene Glycol, Hydrogenated Lecithin, Caprylyl Glycol, Fragaria Vesca (Strawberry) Fruti Extract, Malus Domesca Fruit Extract, Vaccinium Macrocarpon (Cranberry) Fruit Extract, Ceramide NP, Punica Granatum Fruit Extract, Cholesterol, Hydroxypropyltrimonium Hyaluronate, Phytosphingosine, Ceramide NG, Ceramide NS, Ceramide AP, Ceramide AS, Hydrolyzed Hyaluronic Acid, Sodium Acetylated Hyaluronic Acid, Hydrolyzed Sodium Hyaluronate, Potassium Hyaluronate, Ceramide EOP, Fragrance. 

Other Information

SPL UNCLASSIFIED SECTION

  • Protect the product in this container from excessive heat and direct sun

Questions or comments?

OTC - QUESTIONS SECTION

Please send an email to the following address skinidea@medipeel.com

Package Labelling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label.jpgPackage Label.jpg

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72220-00072220-000-00

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 48 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
1d7467dc-6983-5e09-e063-6294a90a3316d122e231-381c-442e-9ea9-d2c85c51d5882024-07-17WarningsExact identifier
spl id: 1d7467dc-6983-5e09-e063-6294a90a3316
spl set id: d122e231-381c-442e-9ea9-d2c85c51d588

Reported adverse events (FAERS/openFDA)#

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