INVISIBLE PHYSICAL DEFENSE SPF30- zinc oxide lotion 
Dermalogica, Inc.

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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INVISIBLE PHYSICAL DEFENSE SPF30

Drug Facts

Active ingredient

Zinc Oxide (20.9%)

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, Caprylic/Capric Triglyceride, C12-15 Alkyl Benzoate, Butyloctyl Salicylate, Dimethicone, Butylene Glycol, Glycerin, Caprylyl Methicone, Silica, Lauryl Peg-9 Polydimethylsiloxyethyl Dimethicone, Argania Spinosa Kernel Oil, Polyhydroxystearic Acid, Octyldodecanol, Sodium Chloride, Cordyceps Sinensis Extract, Poria Cocos Sclerotium Extract, Camellia Sinensis Leaf Extract, Lavandula Angustifolia (Lavender) Flower Extract, Lavandula Hybrida Oil, Tocopheryl Acetate, PEG-10 Dimethicone, Pentylene Glycol, Caprylyl Glycol, Ethylhexylglycerin, Bisabolol, Sodium Hyaluronate, Xylose, Dimethicone Crosspolymer, Sorbitan Olivate, Octyldodecyl Xyloside, PEG-30 Dipolyhydroxystearate, Eucalyptol, Xanthan Gum, Tocopherol, Sodium Citrate, Sodium Hydroxide, Propanediol, Stearalkonium Hectorite, Propylene Carbonate, Potassium Sorbate, Sodium Benzoate, Linalool, Limonene.

Questions or comments

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

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton

dermalogica

invisible
physical
defense

SPF
30
FPS

broad spectrum

weightless
physical
sunscreen

Aust L 335173

1.7 US FL OZ / 50 mL e

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton
INVISIBLE PHYSICAL DEFENSE SPF30 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68479-991
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide20.9 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Medium-Chain Triglycerides (UNII: C9H2L21V7U)  
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)  
Butyloctyl Salicylate (UNII: 2EH13UN8D3)  
Dimethicone (UNII: 92RU3N3Y1O)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Glycerin (UNII: PDC6A3C0OX)  
Caprylyl Trisiloxane (UNII: Q95M2P1KJL)  
Silicon Dioxide (UNII: ETJ7Z6XBU4)  
Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone (UNII: 25G622K2RA)  
Argan Oil (UNII: 4V59G5UW9X)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
Octyldodecanol (UNII: 461N1O614Y)  
Sodium Chloride (UNII: 451W47IQ8X)  
Sorbitan Olivate (UNII: MDL271E3GR)  
.Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0)  
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
Pentylene Glycol (UNII: 50C1307PZG)  
Propanediol (UNII: 5965N8W85T)  
Octyldodecyl Xyloside (UNII: 8Z6VNR46QM)  
Peg-30 Dipolyhydroxystearate (4000 Mw) (UNII: 9713Q0S7FO)  
Stearalkonium Hectorite (UNII: OLX698AH5P)  
Caprylyl Glycol (UNII: 00YIU5438U)  
Xanthan Gum (UNII: TTV12P4NEE)  
Ophiocordyceps Sinensis (UNII: 8Q1GYP08KU)  
FU LING (UNII: XH37TWY5O4)  
Sodium Citrate, Unspecified Form (UNII: 1Q73Q2JULR)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Propylene Carbonate (UNII: 8D08K3S51E)  
Lavandin Oil (UNII: 9RES347CKG)  
Levomenol (UNII: 24WE03BX2T)  
Hyaluronate Sodium (UNII: YSE9PPT4TH)  
Green Tea Leaf (UNII: W2ZU1RY8B0)  
Potassium Sorbate (UNII: 1VPU26JZZ4)  
Eucalyptol (UNII: RV6J6604TK)  
Sodium Benzoate (UNII: OJ245FE5EU)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Xylose (UNII: A1TA934AKO)  
Lavandula Angustifolia Subsp. Angustifolia Flower (UNII: 19AH1RAF4M)  
Tocopherol (UNII: R0ZB2556P8)  
Linalool, (+/-)- (UNII: D81QY6I88E)  
Limonene, (+)- (UNII: GFD7C86Q1W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68479-991-021 in 1 CARTON01/01/2022
150 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:68479-991-04177 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2022
3NDC:68479-991-057 mL in 1 TUBE; Type 0: Not a Combination Product01/01/2022
4NDC:68479-991-002 mL in 1 POUCH; Type 0: Not a Combination Product01/01/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35201/01/2022
Labeler - Dermalogica, Inc. (177698560)
Establishment
NameAddressID/FEIBusiness Operations
McKenna090631412MANUFACTURE(68479-991)

Revised: 4/2022
Document Id: 7c9b996d-94d7-4522-8a05-9319e797dd64
Set id: 2e5e6861-25ea-4605-8e59-41d852c002b7
Version: 2
Effective Time: 20220420
 
Dermalogica, Inc.