PORESCREEN SPF40- zinc oxide lotion 
Dermalogica, LLC.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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PORESCREEN SPF40

Drug Facts

Active ingredients

Zinc Oxide (10%)

Purpose

Sunscreen

Uses

Warnings

For external use only

Do not use

  • on damaged or broken skin.

When using this product

  • keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor

  • if rash occurs.

Keep out of reach of children.

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

Directions

Other information

Inactive ingredients

Water/Aqua/Eau, C12-15 Alkyl Benzoate, Octyldodecyl Neopentanoate, Butyloctyl Salicylate, Caprylic/Capric Triglyceride, Isododecane, Lauryl PEG-8 Dimethicone, Propanediol, Niacinamide, Methylpropanediol, Titanium Dioxide (CI 77891), Silica Silylate, Lactic Acid, Helianthus Annuus (Sunflower) Seed Oil, Lavandula Angustifolia (Lavender) Flower/Leaf/Stem Extract, Chamomilla Recutita (Matricaria) Flower Extract, Rosa Damascena Extract, Chlorella Vulgaris Extract, Sea Salt (Maris Sal), Olive Oil Decyl Esters, Squalene, Tocopherol, Caprylyl Glycol, Lecithin, Allantoin, Propylene Glycol Stearate, Glycerin, Bisabolol, Lauryl PEG-10 Tris(Trimethylsiloxy)silylethyl Dimethicone, PEG-10, Silica, Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate, Magnesium Stearate, Tetrasodium Glutamate Diacetate, Citric Acid, Sodium Hydroxide, Sodium Chloride, Bentonite, Cellulose Acetate, Phenylpropanol, Hydrated Silica, Acrylates/Ammonium Methacrylate Copolymer, Iron Oxides (CI 77491, CI 77492, CI 77499), Linalool.

Questions or comments?

Call toll free 1-800-831-5150 in the US.

PRINCIPAL DISPLAY PANEL - 30 mL Tube Carton

dermalogica

porescreen

SPF
40

high
protection

UVA
UVB

broad spectrum

with
niacinamide

blurring + hint of tint
mineral sunscreen

Sun Care

1.0 US FL OZ / 30 mL ℮

Principal Display Panel - 30 mL Tube Carton
PORESCREEN SPF40 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68479-291
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide10 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
Octyldodecyl Neopentanoate (UNII: X8725R883T)  
Butyloctyl Salicylate (UNII: 2EH13UN8D3)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
Isododecane (UNII: A8289P68Y2)  
Propanediol (UNII: 5965N8W85T)  
Methylpropanediol (UNII: N8F53B3R4R)  
Niacinamide (UNII: 25X51I8RD4)  
Titanium Dioxide (UNII: 15FIX9V2JP)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
Polyglyceryl-4 Diisostearate/Polyhydroxystearate/Sebacate (UNII: 687U3PEB2Y)  
Sodium Chloride (UNII: 451W47IQ8X)  
Bentonite (UNII: A3N5ZCN45C)  
Caprylyl Glycol (UNII: 00YIU5438U)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
SUNFLOWER OIL (UNII: 3W1JG795YI)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
Allantoin (UNII: 344S277G0Z)  
Cellulose Acetate (UNII: 3J2P07GVB6)  
Olive Oil Decyl Esters (UNII: 3AQ222F18X)  
Phenylpropanol (UNII: 0F897O3O4M)  
PROPYLENE GLYCOL MONOSTEARATE (UNII: MZM1I680W0)  
Magnesium Stearate (UNII: 70097M6I30)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Glycerin (UNII: PDC6A3C0OX)  
Hydrated Silica (UNII: Y6O7T4G8P9)  
POLYETHYLENE OXIDE 200000 (UNII: 11628IH70O)  
Tetrasodium Glutamate Diacetate (UNII: 5EHL50I4MY)  
LACTIC ACID, DL- (UNII: 3B8D35Y7S4)  
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWERING TOP (UNII: 9YT4B71U8P)  
LEVOMENOL (UNII: 24WE03BX2T)  
Squalene (UNII: 7QWM220FJH)  
MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)  
ROSA X ALBA FLOWER OIL (UNII: FF1Y064QVO)  
CHLORELLA VULGARIS (UNII: RYQ4R60M02)  
Sea Salt (UNII: 87GE52P74G)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Tocopherol (UNII: R0ZB2556P8)  
LINALOOL, (+/-)- (UNII: D81QY6I88E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68479-291-021 in 1 CARTON12/01/2022
130 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:68479-291-0459 mL in 1 TUBE; Type 0: Not a Combination Product12/01/2022
3NDC:68479-291-055 mL in 1 TUBE; Type 0: Not a Combination Product12/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35212/01/2022
Labeler - Dermalogica, LLC. (177698560)
Establishment
NameAddressID/FEIBusiness Operations
Nanophase Technologies623502044MANUFACTURE(68479-291)

Revised: 12/2022
Document Id: 4a597566-2390-4f4e-bc17-1950aa54222f
Set id: 37a7362a-b251-4d3a-a957-65d8f338fa12
Version: 3
Effective Time: 20221221
 
Dermalogica, LLC.