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 - 7.50%
Octisalate - 5.00%
Oxybenzone - 3.00%
Otc - Purpose
Octinoxate - 7.50% .....................Sunscreen.
Octisalate - 5.00% ......................Sunscreen.
Oxybenzone - 3.00% ..................Sunscre.en.
Indications & Usage
Use • helps prevent sunburn.
Warnings
Warnings
Skin cancer/Skin Aging alert
For external use only
Do noy use on Damage or broken skin
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 a 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, Cyclohexasiloxanel, Cyclopentasiloxane
Dimethicone Crosspolymer, Fragrance, Hydrogenated Polyisobutene, Hydrolyzed Jojoba Esters, Jojoba Esters, Juglans Regia (Walnut) Seed Oil, Mineral OilSorbitan Olivate, Tocopheryl Acetatel, Water
Package Label.Principal Display Panel
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