Active Ingredients
Octinoxate 7.5%
Oxybenzone 4.5%
Walgreens Sunscreen
FDA Label NDC 0363-4001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Co. for the product Walgreens Sunscreen (NDC 0363-4001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of the reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Sunscreen
Uses
- helps prevent sunburn
- higher SPF gives more sunburn protection
- retains SPF after 80 minutes of activity in the water
Warnings
For external use only
When Using This Product
- keep out of eyes. Rinse with water to remove.
Stop Use And Ask A Doctor If
- rash or irritation develops and lasts.
Keep Out Of The Reach Of Children.
If swallowed get medical help or contact a Poison Control Center right away.
Directions
- apply generously and evenly before sun exposure and as needed
- children under 6 months of age:ask a doctor
- reapply frequently and after towel drying, swimming or perspiring.
Inactive Ingredients
Water, Stearic Acid, Sorbitol, Sorbitan Oleate, Glyceryl Stearate SE, Hydrogenated Vegetable oil Isopropyl Myristate, Triethanolamine,VP/Eicosene Copolymer, Benzyl Alcohol, Imadazolidinyl Urea, Methylparaben, Dimethicone,Carbomer, Fragrance,Simmondsia Chinensis(Jojoba) Seed Oil, Propylparaben, Tocopherol, Aloe Barbadensis Leaf Juice, Disodium EDTA.
Principal Display Panel
Mix and Match $2.99 each2/$5WalgreensSUNSCREENLOTIONUVA/UVBPROTECTIONVERY WATER RESISTANTSPF153 FL OZ (89 mL)
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