FDA.reportPublic FDA data

Veil Fluid Makeup Ivory

Manufacturer
Kingdom Animalia, LLC. DBA Hourglass Cosmetics
Effective date
2020-12-08
Label type
HUMAN OTC DRUG LABEL
Version
22
Source
legacy-cache
Hydrated at
2026-08-01 23:03:36

Label at a glance#

ProductVeil Fluid Makeup Ivory SPF 15
Active ingredientOCTINOXATE, OCTISALATE, OXYBENZONE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients               Purpose
Octinoxate  7.5%                          Sunscreen
Octisalate  4.0%                           Sunscreen
Oxybenzone 3.0%                         Sunscreen

OTC - PURPOSE SECTION

Enter section text here

INDICATIONS & USAGE SECTION

Uses
  • helps prevent sunburn
  • if used as directed with other sun protection measures (see Directions), decrease the risk of skin cancer and early skin aging cause by the sun.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on damage or broken skin.

OTC - WHEN USING SECTION

When using this product keep out of eyes.  If contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop Use and ask a doctor if irritation or rash develops.

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.

INSTRUCTIONS FOR USE SECTION

Directions

  • SHAKE WELL, and apply to moisturized or primed skin with fingertips or Hourglass Foundation Brush.
  • 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 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 INGREDIENT SECTION

Inactive Ingredients  CETEARYL ETHYLHEXANOATE, CETYL PEG/PPG 10/1 DIMETHICONE, CYCLOPENTASILOXANE, DIMETHICONE, ETHYLHEXYLGLYCERIN, GLYCERIN, GLYCERYL BEHENATE, GLYCERYL DIBEHENATE, HDI/TRIMETHYLOL HEXYLLACTONE CROSS-POLYMER, HEXYL LAURATE, HYDROLYZED WHEAT PROTEIN, HYDOXYPROPYL CYCLODEXTRIN, ISODODECANE, ISOEICOSANE, MACROCYSTIC PYRIFERA EXTRACT, MAGNESIUM SULFATE, PALMITOYL TRIPEPTIDE-38, PENTAERYTHRITYL TETRAISOSTEARATE, PHENOXYETHANOL, PHENYL TRIMETHICONE, POLYGLYCERYL-4 ISOSTEARATE, POTASSIUM SORBATE, PROPYLENE CARBONATE, PVP, QUATERNIUM-90 BENTONITE, SILICA, SODIUM BENZOATE, TOCOPHERYL ACETATE, TRIBEHENIN, TRIETHOXYLCAPRYLYLSILANE, WATER. MAY CONTAIN (+/-): IRON OXIDES (CI 77491), IRON OXIDES (CI 77492), IRON OXIDES (CI 77499), TITANIUM DIOXIDE (CI 77891).

OTHER SAFETY INFORMATION

Other Information

Protect this product from excessive heat and direct sun.

OTC - QUESTIONS SECTION

Questions or comments?

CALL TOLL FREE 855-201-4529

HOW SUPPLIED SECTION

DIST. BY KINGDOM ANIMALIA, LLC.  VENICE, CA 90291  USA
HOURGLASS COSMETICS, UK LTD, LONDON WC1D 3JA
MADE IN USA   PRODUCT NOT TESTED ON ANIMALS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VeilFluidMUVeilFluidMU

Products#

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

DailyMed product names page 1 of 1 · 36 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42627-20242627-202-01, 42627-202-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 34 matching rows.

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
OXYBENZONE95OOS7VE0YACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
MAGNESIUM SULFATE, UNSPECIFIEDDE08037SABIACT
PALMITOYL TRIPEPTIDE-52A3916MQHOIACT
HYDROLYZED WHEAT PROTEIN (ENZYMATIC, 3000 MW)J2S07SB0YLIACT
PHENOXYETHANOLHIE492ZZ3TIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
BIOTIN6SO6U10H04IACT
EDETATE TRISODIUM420IP921MBIACT
SODIUM BENZOATEOJ245FE5EUIACT
POLYGLYCERYL-4 ISOSTEARATE820DPX33S7IACT
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5)035JKJ76MTIACT
HEXYL LAURATE4CG9F9W01QIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
GLYCERYL DIBEHENATER8WTH25YS2IACT
TRIBEHENIN8OC9U7TQZ0IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ISODODECANEA8289P68Y2IACT
QUATERNIUM-9100J8H295NBIACT
PROPYLENE CARBONATE8D08K3S51EIACT
CYCLOMETHICONE 50THT5PCI0RIACT
DIMETHICONE92RU3N3Y1OIACT
CETEARYL ETHYLHEXANOATE9M64UO4C25IACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
PENTAERYTHRITYL TETRAISOSTEARATE9D7IK5483FIACT
ISOEICOSANEAR294KAG3TIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
FERRIC OXIDE YELLOWEX438O2MRTIACT
FERRIC OXIDE RED1K09F3G675IACT
FERROSOFERRIC OXIDEXM0M87F357IACT

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
3f3a13f8-7164-4c59-8885-c072a4d9ff9eace49e55-4d24-424d-895c-762fca43b40e2020-12-08WarningsExact identifier
spl id: 3f3a13f8-7164-4c59-8885-c072a4d9ff9e
spl set id: ace49e55-4d24-424d-895c-762fca43b40e

Reported adverse events (FAERS/openFDA)#

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