FDA.reportPublic FDA data

Q Skin PLD Sunshade

Manufacturer
International Cosmeceuticals, Inc
Effective date
2026-08-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-28 00:01:51

Label at a glance#

ProductQ Skin Science
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure9 sections

Dosage and administration

Apply evenly to skin 15 minutes before sun exposure. Reapply as needed or after towel drying or swimming For children under 6 months, ask doctor Reapply at least every 2 hours Use a water resistant sunscreen if swimming or sweating

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide................10.9%

Zinc Oxide.........................4.01%

INDICATIONS & USAGE 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

OTC - PURPOSE SECTION

Sunscreen

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Warnings

WARNINGS SECTION

• For external use only. * Do not use or damaged or broken skin. • Keep out of eyes, rinse with water to remove. If skin irritation or rash develops, discontinue use. For children under 6 months of age, ask a doctor before use.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply evenly to skin 15 minutes before sun exposure.
  • Reapply as needed or after towel drying or swimming
  • For children under 6 months, ask doctor
  • Reapply at least every 2 hours
  • Use a water resistant sunscreen if swimming or sweating

Other Ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Cyclotetrasiloxane, Dimethicone/Vinyl, Dimethicone Crosspolymer, Methyl Methacrylate/Glycol Dimethacrylate Crosspolymer, Camellia Sinensis Leaf Extract (Green Tea), Calcium Behenate, Alumina, Dimethiconol, Iron Oxides, Melanin, Ascorbyl Linoleate, Sorbitan Isostearate, Miristoyl Nonapeptide-3, Miristoyl Pentapeptide-17, Methicone, Tribehenin, PEG-10 Dimethicone, Silybin, Tocopheryl Linoleate

Other Information

OTHER SAFETY INFORMATION

Protect the product in thsi container from excessive heat and direct sun.

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65582-83965582-839-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
CYCLOPENTASILOXANE0THT5PCI0RIACT
CALCIUM BEHENATEJ5VFA9V6YGIACT
DIMETHICONOL (14000 CST)M2HW98ZA4VIACT
DIMETHICONE CROSSPOLYMERUF7620L1W6IACT
SORBITAN ISOSTEARATE01S2G2C1E4IACT
MYRISTOYL PENTAPEPTIDE-17AMR73HY95QIACT
TRIBEHENIN8OC9U7TQZ0IACT
MELANIN SYNTHETIC (TYROSINE, PEROXIDE)O0CV1RMR44IACT
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
BROWN IRON OXIDE1N032N7MFOIACT
CYCLOTETRASILOXANECZ227117JEIACT
ALUMINALMI26O6933IACT
ASCORBYL LINOLEATEZ54S26111BIACT
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMEREG97988M5QIACT
DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE)9E4CO0W6C5IACT
CAMELLIA SINENSIS LEAF OILVC855RRT77IACT
SILYBIN4RKY41TBTFIACT

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
Q Skin ScienceSUNSCREENInternational Cosmeceuticals, Inc59e4c3d0-ee4c-2350-e063-6394a90ac9d22026-08-25WarningsExact identifier
ndc (package): 65582-839-50
ndc (product): 65582-839
ndc11 (package): 65582083950
spl id: 59e4c402-7586-7998-e063-6294a90a1440
spl set id: 59e4c3d0-ee4c-2350-e063-6394a90ac9d2

Reported adverse events (FAERS/openFDA)#

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