FDA.reportPublic FDA data

Skinprint Ultra Sheer SPF 20

Manufacturer
The Skin Atelier, Inc.
Effective date
2010-10-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:09:49

Label at a glance#

ProductSkinprint Ultra Sheer SPF 20
Active ingredientHOMOSALATE, OXYBENZONE, OCTISALATE, ENSULIZOLE, OCTOCRYLENE, AVOBENZONE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: 15% HOMOSALATE, 5% BENZOPHENONE-3, 5% ETHYLHEXYL SALICYLATE, 4% PHENYLBENZIMIDAZOLE SULPHONIC ACID, 3% BUTYL METHOXYDIBENZOLYMETHANE, 2.7% OCTOCRYLENE

INSTRUCTIONS FOR USE SECTION

Apply daily to the face and neck as the last step in your daily skin care routine.

DOSAGE & ADMINISTRATION SECTION

Apply daily to the face and neck as the last step in your daily skin care routine.

WARNINGS SECTION

Warning: For external use only. When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water. Keep out of the reach of children. If swallowed get medical help or contact Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warning: For external use only. When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water. Keep out of the reach of children. If swallowed get medical help or contact Poison Control Center right away.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: DISTILLED WATER, CYCLOPENTASILOXANE, DIMETHICONE CROSSPOLYMER, DIMETHICONE, LAURETH-23, LAURETH-4, POLYACRYLAMIDE, C-13 14 ISOPARAFIN, LAURETH-4, TRIETHANOLAMINE, GLYCERIN, PHENOXYETHANOL, CAPRYLYL GLYCOL, POTASSIUM SORBATE, HEXYLENE GLYCOL, BISABOLOL, ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT, POLYSILICONE-15, BUTYLATED HYDROXYTOLUENE, DISODIUM EDTA, FRAGRANCE, GLYCOLIC ACID

INDICATIONS & USAGE SECTION

UVA and UVB sun protection with a SPF of 50 formulated for daily facial use.

OTC - PURPOSE SECTION

UVA and UVB sun protection with a SPF of 50 formulated for daily facial use.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label_Reflect copy.jpgLabel_Reflect copy.jpg

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71393-01271393-012-50, 71393-012-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 matching rows.

Name, UNII, Kind table
NameUNIIKind
POTASSIUM SORBATE1VPU26JZZ4IACT
HOMOSALATEV06SV4M95SACTIB
DIMETHICONE 200RGS4T2AS00IACT
LAURETH-7Z95S6G8201IACT
OXYBENZONE95OOS7VE0YACTIB
OCTISALATE4X49Y0596WACTIB
ENSULIZOLE9YQ9DI1W42ACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMERRSA9I561OKIACT
GLYCOLIC ACID0WT12SX38SIACT
OCTOCRYLENE5A68WGF6WMACTIB
GLYCERINPDC6A3C0OXIACT
CAPRYLYL GLYCOL00YIU5438UIACT
POLYSILICONE-15F8DRP5BB29IACT
MAGNESIUM DISODIUM EDTANDT563S5VZIACT
AVOBENZONEG63QQF2NOXACTIB
WATER059QF0KO0RIACT
LAURETH-23N72LMW566GIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
.ALPHA.-BISABOLOL, (+/-)-36HQN158VCIACT
ZINGIBER OFFICINALE WHOLEIN6Q3S3414IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
TROLAMINE9O3K93S3TKIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
5f0df3d2-dc93-1113-e053-2991aa0a2b7d5f0df3d2-dc92-1113-e053-2991aa0a2b7d2010-10-06WarningsExact identifier
spl id: 5f0df3d2-dc93-1113-e053-2991aa0a2b7d
spl set id: 5f0df3d2-dc92-1113-e053-2991aa0a2b7d

Reported adverse events (FAERS/openFDA)#

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