DAILY DEFENSE  SPF 15- avobenzone, octinoxate, octisalate, and oxybenzone 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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Daily Defense
SPF 15

Drug Facts

Active Ingredients

Avobenzone (3.0%), Octinoxate (6.5%), Octisalate (3.0%), Oxybenzone (3.5%).

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

Inactive ingredients

Water/Aqua/Eau, Butylene Glycol, Caprylic/Capric Triglyceride, Glyceryl Stearate, Cetearyl Phosphate, Glycerin, Stearic Acid, Polyglyceryl-2 Stearate, Dimethicone, Lactamide MEA, Pyrus Malus (Apple) Fruit Extract, Dimethyl Capramide, Mahonia Aquifolium Root Extract, Lavandula Angustifolia (Lavender) Extract, Hydrolyzed Opuntia Ficus Indica Flower Extract, Triticum Vulgare (Wheat) Germ Extract, Saccharomyces Cerevisiae Extract, Lavandula Spica (Lavender) Flower Oil, Lavandula Hybrida Oil, Eucalyptus Globulus Leaf Oil, Sodium Hyaluronate, Dipotassium Glycyrrhizate, Palmitoyl Tripeptide-5, Sodium DNA, Tocopherol, Allantoin, Panthenol, Glycerin Crosspolymer, Ascorbyl Tetraisopalmitate, Carbomer, Polyquaternium-10, Cetyl Alcohol, Xanthan Gum, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Disodium EDTA, Citric Acid, Potassium Sorbate, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol.

Other information

Questions or comments

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

PRINCIPAL DISPLAY PANEL - 100 mL Tube Carton

daily
defense

spf
15
broad
spectrum

dermalogica®

3.4 US FL OZ
100 mL e

Principal Display Panel - 100 mL Tube Carton
DAILY DEFENSE   SPF 15
avobenzone, octinoxate, octisalate, and oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68479-800
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone30 mg  in 1 mL
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51) Octinoxate65 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate30 mg  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone35 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Butylene Glycol (UNII: 3XUS85K0RA)  
Medium-Chain Triglycerides (UNII: C9H2L21V7U)  
Glyceryl Monostearate (UNII: 230OU9XXE4)  
Cetyl Phosphate (UNII: VT07D6X67O)  
Glycerin (UNII: PDC6A3C0OX)  
Stearic Acid (UNII: 4ELV7Z65AP)  
Dimethicone (UNII: 92RU3N3Y1O)  
N-Lactoyl Ethanolamine (UNII: 900T44YNC7)  
Apple (UNII: B423VGH5S9)  
Dimethyl Capramide (UNII: O29Y6X2JEZ)  
Mahonia Aquifolium Root (UNII: 746TB9VNDP)  
Lavandula Angustifolia Flowering Top (UNII: 9YT4B71U8P)  
Vitis Vinifera Seed (UNII: C34U15ICXA)  
Wheat Germ (UNII: YR3G369F5A)  
Saccharomyces Cerevisiae (UNII: 978D8U419H)  
Hyaluronate Sodium (UNII: YSE9PPT4TH)  
Phenoxyethanol (UNII: HIE492ZZ3T)  
Cetyl Alcohol (UNII: 936JST6JCN)  
Panthenol (UNII: WV9CM0O67Z)  
Lavender Oil (UNII: ZBP1YXW0H8)  
Lavandin Oil (UNII: 9RES347CKG)  
Eucalyptus Oil (UNII: 2R04ONI662)  
Ascorbyl Tetraisopalmitate (UNII: 47143LT58A)  
Tocopherol (UNII: R0ZB2556P8)  
Allantoin (UNII: 344S277G0Z)  
Palmitoyl Tripeptide-5 (UNII: 2A3916MQHO)  
Carbomer Homopolymer Type C (Allyl Pentaerythritol Crosslinked) (UNII: 4Q93RCW27E)  
Sodium NA-22 (UNII: N2511Z637B)  
Edetate Disodium (UNII: 7FLD91C86K)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Glycyrrhizinate Dipotassium (UNII: CA2Y0FE3FX)  
Polidronium Chloride (UNII: 6716Z5YR3G)  
Egg Phospholipids (UNII: 1Z74184RGV)  
Aminomethylpropanol (UNII: LU49E6626Q)  
Citric Acid Monohydrate (UNII: 2968PHW8QP)  
Xanthan Gum (UNII: TTV12P4NEE)  
Carbomer Interpolymer Type A (Allyl Sucrose Crosslinked) (UNII: 59TL3WG5CO)  
Caprylyl Glycol (UNII: 00YIU5438U)  
Hexylene Glycol (UNII: KEH0A3F75J)  
Potassium Sorbate (UNII: 1VPU26JZZ4)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68479-800-021 in 1 CARTON
1100 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:68479-800-002 mL in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35204/13/2012
Labeler - Dermalogica, Inc. (177698560)
Establishment
NameAddressID/FEIBusiness Operations
Cosway620899877MANUFACTURE(68479-800)
Establishment
NameAddressID/FEIBusiness Operations
Diamond Wipes161104729MANUFACTURE(68479-800)

Revised: 11/2015
Document Id: a42ae7d9-be11-4911-aec3-a78921bda29a
Set id: 28e4e1f8-48df-49fb-a702-d1e5b602067c
Version: 2
Effective Time: 20151118
 
Dermalogica, Inc.