INVISIBLE PHYSICAL DEFENSE SPF 30- 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 SPF 30

Drug Facts

Active ingredient

Zinc Oxide (20%)

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, Dimethicone, Butyloctyl Salicylate, Butylene Glycol, Glycerin, Silica, Polyhydroxystearic Acid, PEG-10 Dimethicone, Argania Spinosa Kernel Oil, Cordyceps Sinensis Extract, Trametes Versicolor Extract, Sodium Hyaluronate, Camellia Sinensis Leaf Extract, Eucalyptus Globulus Leaf Oil, Lavandula Spica (Lavender) Flower Oil, Tocopheryl Acetate, Sodium Chloride, Stearalkonium Hectorite, Pentylene Glycol, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Propanediol, Dimethicone Crosspolymer, Sodium Citrate, Propylene Carbonate, Xanthan Gum, Caprylyl Glycol, Bisabolol, Lavandula Hybrida Oil, Ethylhexylglycerin, Sodium Hydroxide, Potassium Sorbate, Sodium Benzoate.

Questions or comments

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

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton

invisible
physical
defense

dermalogica

SPF
30

broad spectrum

weightless
physical
sunscreen

1.7 US FL OZ / 50 mL ℮

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton
INVISIBLE PHYSICAL DEFENSE SPF 30 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68479-909
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide200 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
Dimethicone (UNII: 92RU3N3Y1O)  
Butyloctyl Salicylate (UNII: 2EH13UN8D3)  
Glycerin (UNII: PDC6A3C0OX)  
Butylene Glycol (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
POLYHYDROXYSTEARIC ACID STEARATE (UNII: 8KQ7I65XZE)  
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
ARGAN OIL (UNII: 4V59G5UW9X)  
OPHIOCORDYCEPS SINENSIS (UNII: 8Q1GYP08KU)  
TRAMETES VERSICOLOR FRUITING BODY (UNII: 4C900477MT)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
LAVENDER OIL (UNII: ZBP1YXW0H8)  
Sodium Chloride (UNII: 451W47IQ8X)  
Stearalkonium Hectorite (UNII: OLX698AH5P)  
Pentylene Glycol (UNII: 50C1307PZG)  
Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone (UNII: 25G622K2RA)  
Propanediol (UNII: 5965N8W85T)  
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
Propylene Carbonate (UNII: 8D08K3S51E)  
Xanthan Gum (UNII: TTV12P4NEE)  
Caprylyl Glycol (UNII: 00YIU5438U)  
LEVOMENOL (UNII: 24WE03BX2T)  
Ethylhexylglycerin (UNII: 147D247K3P)  
LAVANDIN OIL (UNII: 9RES347CKG)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Potassium Sorbate (UNII: 1VPU26JZZ4)  
Sodium Benzoate (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68479-909-011 in 1 CARTON03/05/2020
17 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:68479-909-0250 mL in 1 TUBE; Type 0: Not a Combination Product03/05/2020
3NDC:68479-909-04177 mL in 1 TUBE; Type 0: Not a Combination Product03/05/2020
4NDC:68479-909-00177 mL in 1 TUBE; Type 0: Not a Combination Product03/05/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35203/05/2020
Labeler - Dermalogica, Inc. (177698560)
Establishment
NameAddressID/FEIBusiness Operations
McKenna090631412MANUFACTURE(68479-909)

Revised: 3/2020
Document Id: bbee87e7-daab-4699-a9ff-f9d22fa5ffe5
Set id: 78355b1d-dd91-42c4-931d-36b8a5b9a546
Version: 1
Effective Time: 20200305
 
Dermalogica, Inc.