FDA Label for Hampton Sun
View Indications, Usage & Precautions
Hampton Sun Product Label
The following document was submitted to the FDA by the labeler of this product Inspec Solutions Llc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Active Ingredients:
Octinoxate – 4.00%
Oxybenzone - 2.00%
Otc - Purpose
Octinoxate – 4.00%..................Sunscreen
Oxybenzone - 2.00%...............Sunscreen
Indications & Usage
Uses • Helps prevent sunburn
Warnings
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.
Otc - Stop Use
Stop use and ask a doctor if rash occurs.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
Dosage & Administration
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 Ingredient
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
Package Label.Principal Display Panel
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