SKINPRINT ULTRA SHEER SPF 20- skinprint ultra sheer spf 20 lotion 
The Skin Atelier, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Active Ingredients: 6% Ethylhexyl methoxycinnamate, 3% Phenylbenzimidazole Sulphonic Acid, 1.5% Butyl Methoxydibenzolymethan, 1.2% Octocrylene

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

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

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.

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.

WATER, CYCLOPENTASILOXANE, DIMETHICONE CROSSPOLYMER, DIMETHICONE, LAURETH-23, LAURETH-4, POLYACRYLAMIDE, C-13 -14 ISOPARAFFIN, LAURETH 7, GLYCERIN, BISABOLOL, ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT, PHENOXYETHANOL, CAPRYLYL GLYCOL, POTASSIUM SORBATE, HEXYLENE GLYCOL, TRIETHANOLAMINE, BUTYLATED HYDROXYTOLUENE, DISODIUM EDTA, FRAGRANCE, GLYCOLIC ACID

UVA and UVB sun protection with a SPF of 20 formulated for daily facial use.

UVA and UVB sun protection with a SPF of 20 formulated for daily facial use.

Label_UltraSheer.jpg

SKINPRINT ULTRA SHEER SPF 20 
skinprint ultra sheer spf 20 lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71393-011
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE6 g  in 100 g
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1.5 g  in 100 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE1.2 g  in 100 g
ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE3 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
LAURETH-23 (UNII: N72LMW566G)  
LAURETH-4 (UNII: 6HQ855798J)  
GLYCERIN (UNII: PDC6A3C0OX)  
ZINGIBER OFFICINALE WHOLE (UNII: IN6Q3S3414)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
TROLAMINE (UNII: 9O3K93S3TK)  
GLYCOLIC ACID (UNII: 0WT12SX38S)  
.ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)  
LAURETH-7 (UNII: Z95S6G8201)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)  
WATER (UNII: 059QF0KO0R)  
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)  
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71393-011-0550 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/06/2009
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other08/06/200910/11/2019
Labeler - The Skin Atelier, Inc. (135049810)
Establishment
NameAddressID/FEIBusiness Operations
The Skin Atelier, Inc.135049810manufacture(71393-011)

Revised: 1/2020
Document Id: 9c58b876-9c86-5807-e053-2995a90a20cb
Set id: 5cf2536d-33fd-6d0e-e053-2991aa0ae486
Version: 2
Effective Time: 20200117
 
The Skin Atelier, Inc.