Paulas Choice DEFENSE Essential Glow Moisturizer SPF 30

Manufacturer
Paula's Choice LLC
Effective date
2022-01-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:18:54

Label at a glance#

ProductPaulas Choice DEFENSE Essential Glow Moisturizer SPF 30
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Zinc Oxide - 6.125%
Titanium Dioxide - 5.25%

INSTRUCTIONS FOR USE SECTION

  • Apply liberally 15 minutes before sun exposure
  • Use a water-resistant sunscreen if swimming or sweating: immediatelly after towel drying; At least every two hours.
  • Children under 6 months of age: Ask a doctor.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Stop use if rash occurs.

OTC - ASK DOCTOR/PHARMACIST 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 - STOP USE SECTION

Stop use if rash occurs

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sun. Store at 20-25C (68-77F)

INACTIVE INGREDIENT SECTION

Water (Aqua), C12-15 Alkyl Benzoate, Glycerin, Isononyl Isononanoate, Butylene Glycol, Cetearyl Alcohol, Potassium Cetyl Phosphate, Dimethicone, Glyceryl Stearate, Glycyrrhiza Glabra (Licorice) Root Extract, Actinidia Chinensis (Kiwi) Fruit Extract, Argania Spinosa Kernel Oil, Tetrapeptide-30, Linoleic Acid, Resveratrol, Ascorbyl Glucoside, Niacinamide, Tocopheryl Acetate, Magnesium Ascorbyl Phosphate, Bisabolol, Tocopherol, Phospholipids, Lecithin, Glycine Soja (Soybean) Sterols, Xanthophylls, Pullulan, Sodium Gluconate, Xanthan Gum, Sclerotium Gum, Alumina, Caprylic/Capric Triglyceride, Citric Acid, Triethoxycaprylylsilane, C13-14 Isoparaffin, Acrylates Copolymer, Polyhydroxystearic Acid, Caprylyl Glycol, Polyacrylamide, Ceteareth-20, Aluminum Stearate, Laureth-7, Ethylhexylglycerin, Phenoxyethanol.

OTC - PURPOSE SECTION

Sunscreen

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DFPDFPPrincipal Display PanelPrincipal Display Panel

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 2 · 46 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76144-22376144-223-02, 76144-223-01

Ingredients#

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

DailyMed ingredient rows page 1 of 2 · 43 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
c54ddd72-5d4b-218c-e053-2995a90a7cee7432df12-382a-7db6-e053-2991aa0a810a2022-01-06WarningsExact identifier
spl id: c54ddd72-5d4b-218c-e053-2995a90a7cee
spl set id: 7432df12-382a-7db6-e053-2991aa0a810a

Reported adverse events (FAERS/openFDA)#

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