Paulas Choice Extra Care Non-Greasy Sunscreen SPF 50

Manufacturer
Paula's Choice, LLC
Effective date
2022-01-06
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-01 22:19:00

Label at a glance#

ProductPaulas Choice Extra Care Non-Greasy Sunscreen SPF 50
Active ingredientOCTISALATE, OCTOCRYLENE, OXYBENZONE, HOMOSALATE, AVOBENZONE
Label structure9 sections

Storage and handling

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

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Homosalate 10.0%

Oxybenzone 6.0%

Octisalate 5.0%

Avobenzone 3.0%

Octocrylene 2.0%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Helps prevent sunburn. Decreases the risk of skin cancer and early skin aging caused by the if used as directed with other sun protection measures (see Directions).

WARNINGS SECTION

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.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - ASK DOCTOR SECTION

Ask a doctor if rash occurs.

OTC - WHEN USING SECTION

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

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.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

DOSAGE & ADMINISTRATION SECTION

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 broad-spectrum sunscreen rated SPF 25 or greater 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 snglasses.

children under 6 months: Ask a doctor.

OTC - ASK DOCTOR SECTION

Children under 6 months: Ask a doctor.

Other Information

STORAGE AND HANDLING SECTION

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Butylene Glycol, PEG-8, Polyethylene, Dimethicone, Silica, Picea Abies (Spruce) Wood Extract, sodium Ascorbyl Phosphate, Retinyl Palmitate, Tocopherol, Tocopheryl Acetate, Titanium Dioxide, Aloe Barbadensis Leaf Juice, Bentonite, Methyl Glycose Sesquistearate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Sodium Polacrylate, Kaolin, Ethylhexylglycerin, Disodium EDTA, Sodium Hydroxide, Chlorphenesin, Phenoxyethanol

RECENT MAJOR CHANGES SECTION

• Dosage and Administration

1-21-2021

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

148ml148mlcarton 2carton 2carton 1carton 1

Products#

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DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76144-23276144-232-01, 76144-232-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 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
c54df1c4-712c-bc46-e053-2995a90ab473b973230d-1ee0-6564-e053-2995a90afb0b2022-01-06WarningsExact identifier
spl id: c54df1c4-712c-bc46-e053-2995a90ab473
spl set id: b973230d-1ee0-6564-e053-2995a90afb0b

Reported adverse events (FAERS/openFDA)#

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