Otc - Active Ingredient
Active Ingredients:
Octinoxate – 4.00%
Oxybenzone - 2.00%
The following Structured Product Label (SPL) was submitted to the FDA by Hampton Sun for the product Hampton Sun (NDC 87170-001). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Active Ingredients:
Octinoxate – 4.00%
Oxybenzone - 2.00%
Octinoxate – 4.00%..................Sunscreen
Oxybenzone - 2.00%...............Sunscreen
Uses • Helps prevent sunburn
Warnings
Skin cancer/Skin Aging alert
For external use only
Do not use on Damage 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 swallowed, get medical help or contact a Poison Control Center immediately.
DIRECTIONS
• Apply liberally 15 minutes before sun exposure.
• Use water resistant sunscreen if swimming or sweating
• Reapply at least every 2 hours
• Children under 6 months of age: ask a doctor
Inactive Ingredients:
Aloe Barbadensis Leaf Extract, Benzotriazolyl Dodecyl p-Cresol, C12-15 Alkyl Benzoate, Cyclohexasiloxane, Cyclopentasiloxane
Dimethicone Crosspolymer, Ethylhexyl Palmitate, Fragrance, Hydrogenated Polyisobutene, Hydrolyzed Jojoba Esters, Jojoba Esters, Juglans Regia (Walnut) Seed Oil, Mineral Oil, Sorbitan Olivate, Tocopheryl Acetate, Water
* Please review the disclaimer below.