Paula's Choice Moisture Boost Daily Restoring Complex Broad Spectrum SPF 30

Paulas Choice Moisture Boost Daily Restoring Complex by

Drug Labeling and Warnings

Paulas Choice Moisture Boost Daily Restoring Complex by is a Otc medication manufactured, distributed, or labeled by Paula's Choice, LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PAULAS CHOICE MOISTURE BOOST DAILY RESTORING COMPLEX- avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion 
Paula's Choice, 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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Paula's Choice Moisture Boost Daily Restoring Complex Broad Spectrum SPF 30

Avobenzone 3.0%

Homosalate 4.0%

Octisalate 4.0%

Octocrylene 2.0%

Oxybenzone 3.0%

Sunscreen

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 product is swallowed, get medical help or contact a Poison Control Center immediately.

Directions

Apply liberally 15 minutes before sun exposure. Reapply:

  • After 80 minutes of swimming or sweating
  • Immediately after towel drying
  • At least every 2 hours

Sun Protection Measures Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen rated SPF of 25 or higher and other sun protection measures including:

  • Limit time in the sun, especially from 10 a.m. - 2 p.m.
  • Wear long-sleeve shirts, pants, hats, and sunglasses

Children under 6 months: Ask a doctor

Protect this product from excessive heat and direct sun. You may report serious adverse reactions to 705 5th Avenue, South, Suite 200, Seattle, WA 98104.

Water, C12-15 Alkyl Benzoate, Butylene Glycol, VP/Eicosene Copolymer, Sodium Cetearyl Sulfate, Sodium Ascorbyl Phosphate, Retinyl Palmitate, Tocopheryl Acetate, Tocopherol, Picea Abies Wood Extract, Aloe Barbadensis (Aloe Vera) Leaf Juice, Methyl Glucose Sesquistearate, Glyceryl Stearate, Cetearyl Alcohol, Dimethicone, Titanium Dioxide, Bentonite, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Ethylhexylglycerin, Sodium Polyacrylate, Disodium EDTA, Sodium Hydroxide, Chlorphenesin, Phenoxyethanol

SampleFullFull

Sample

PAULAS CHOICE MOISTURE BOOST DAILY RESTORING COMPLEX 
avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 76144-162
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE40 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE30 mg  in 1 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE40 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)  
SODIUM CETOSTEARYL SULFATE (UNII: 7ZBS06BH4B)  
.ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01)  
METHYL GLUCOSE SESQUISTEARATE (UNII: V1YW10H14D)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
BENTONITE (UNII: A3N5ZCN45C)  
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
WATER (UNII: 059QF0KO0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
PICEA ABIES WOOD (UNII: 72GZ8K8996)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76144-162-0060 mL in 1 TUBE; Type 0: Not a Combination Product07/29/2010
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35207/29/201001/12/2022
Labeler - Paula's Choice, LLC. (029583981)

Revised: 3/2023
 

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