Exchange Select Sunscreen
FDA Label NDC 55301-001
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Army And Air Force Exchange Service for the product Exchange Select Sunscreen (NDC 55301-001). 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 before sun exposure and as needed
- children under 6 months of age:ask a doctor
- reapply frequently and after towel drying, swimming or perspiring.
Other Information
- May stain some fabrics
- Sun Alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cance, and other harmful effects of the sun.
Inactive Ingredients
Water, Sorbitan Isostearate, Sorbitol, Triethanolamine, Octadecene/MA Copolymer, Polyglyceryl-3 Distearate, VP/Eicosene Copolymer, Benzyl Alcohol, Barium Sulfate, Dimethicone, Stearic Acid, Carbomer, Phenethyl Alcohol, Simmondsia Chinensis (Jojoba) Seed Oil, Tocopherol, Disodium EDTA, Aloe Barbadensis Leaf Juice Powder, Methylparaben, Propylparaben.
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