Active Ingredients
Avobenzone (3.0%), Homosalate (5.0%), Octinoxate (7.5%), Octisalate (6.5%), Titanium Dioxide (2.0%).
Sunspray
FDA Label NDC 65364-218
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kiss My Face, Llc for the product Sunspray (NDC 65364-218). 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, inactive ingredients, keep out of reach of children, directions, use, purpose, warnings, package display, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredients
Aloe Barbadensis Leaf Juice, Camellia Sinensis (Green Tea) Extract, Carthamus Tinctorius (Safflower) Oleosomes, Cetearyl Alcohol, Cetearyl Olivate, Citric Acid, Daucus Carota Sativa (Carrot) Extract, Dimethicone, Ethylhexylglycerin, Eucalyptus Globulus Oil, Glycerin, Helianthus Annuus (Sunflower) Oil, Lecithin, Phenoxyethanol, Polysorbate-20, Sorbitan Olivate, Styrene/Acrylates Copolymer, Water, Zemea Propanediol.
Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
Apply liberally 15 minutes before sun exposure
Do not spray directly on face
Reapply ater 80 minutes of swimming or sweating, immediately after towel drying, at least ever 2 hours
Children under 6 months ask a doctor
Use
Helps prevent sunburn
Purpose
sunscreen
Warnings
Do not use on damaged or broken skin
Stop use and ask doctor if rash occurs
When using this product keep out of eyes. Rinse with water to remove.
If swallowed get medical help or contact a poison control center right away
* Please review the disclaimer below.
