DAILY DEFENSE SPF 50- face sunscreen lotion 
CP Skin Health Group, Inc.

----------

PCA Skincare Daily Defense SPF 50

Active Ingredients

Octisalate (4.9%)

Octocrylene (9.5%)

Zinc Oxide (9.1%)

Purpose

Sunscreen

Uses

Helps prevent sunburn

If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Warnings

For external use only

Do not use on damaged or broken skin

Stop use and ask a doctor if skin rash occurs

When using this product keep out of eyes. Rinse with water to remove.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

Directions

-Apply liberally 15 minutes before sun exposure

- Use a water resistant sunscreen if swimming or sweating

-Reapply at least every two hours

-Children under 6 months: ask a doctor

-Sun Protectin Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF value of 15 or higher and other skin protecting measures including:

Other informaiton

Protect this product from excessive heat and direct sun

Inactive ingredients

Avena Sativa (Oat) Bran Extract

Bisabolol

Butylene Glycol

Butyloctyl Salicylate

Caffeine

Caprylyl Methicone

Citrus Aurantium Dulcis (Orange) Peel Extract

Cyclopentasiloxane

Ectoin

Ethyl Ferulate

Ethylhexylglycerin

Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer

Octyldodecyl Neopentanoate

Oleth-3 Phosphate

PEG-7 Trimethylolpropane Coconut Ether

Phenoxyethanol

Polyisobutene

Propanediol

Silybum Marianum Seed Extract

Sodium Hyaluronate

Sodium Stearoyl Glutamate

Tocopheryl Acetate

Triethoxycaprylylsilane

Water

Questions or Comments?

877.722.7546

Daily Defense

Daily Defense

DAILY DEFENSE  SPF 50
face sunscreen lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68726-265
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE9.1 g  in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CAFFEINE (UNII: 3G6A5W338E)  
OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
ETHYL FERULATE (UNII: 5B8915UELW)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
WATER (UNII: 059QF0KO0R)  
ORANGE PEEL (UNII: TI9T76XD44)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
PROPANEDIOL (UNII: 5965N8W85T)  
ECTOINE (UNII: 7GXZ3858RY)  
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)  
POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)  
SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
LEVOMENOL (UNII: 24WE03BX2T)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
MILK THISTLE (UNII: U946SH95EE)  
OAT BRAN (UNII: KQX236OK4U)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68726-265-1150 mL in 1 TUBE; Type 0: Not a Combination Product05/01/2020
2NDC:68726-265-377.4 mL in 1 TUBE; Type 0: Not a Combination Product05/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02005/01/2020
Labeler - CP Skin Health Group, Inc. (611921669)

Revised: 2/2024
Document Id: 115b063b-1ecd-7be9-e063-6294a90a2644
Set id: b7b5bfb2-996a-1b3e-e053-2a95a90a976c
Version: 6
Effective Time: 20240214
 
CP Skin Health Group, Inc.