Paulas Choice Moisture Boost Daily Restoring Complex

Manufacturer
Paula's Choice, LLC.
Effective date
2021-06-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:43:46

Label at a glance#

ProductPaulas Choice Moisture Boost Daily Restoring Complex
Active ingredientOCTISALATE, OCTOCRYLENE, HOMOSALATE, OXYBENZONE, AVOBENZONE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%

Homosalate 4.0%

Octisalate 4.0%

Octocrylene 2.0%

Oxybenzone 3.0%

OTC - PURPOSE SECTION

Sunscreen

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INSTRUCTIONS FOR USE SECTION

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

OTHER SAFETY INFORMATION

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.

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ArtworkArtwork

FDA-Initiated Inactive NDC Indexing#

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76144-16276144-162-01, 76144-162-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 29 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
f66f9afb-64cc-79c2-e053-2a95a90aa2eb19aff0f8-7230-56c1-e054-00144ff8d46c2023-03-08WarningsExact identifier
spl set id: 19aff0f8-7230-56c1-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.