Otc - Active Ingredient
AVOBENZONE 3.0%, HOMOSALATE 15.0%, OCTISALATE 5.0%, OCTOCRYLENE 2.8%,
OXYBENZONE 6.0%
The following Structured Product Label (SPL) was submitted to the FDA by Ulta for the product Ulta Sun Dry Touch Spf 70 (NDC 62296-8900). 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, purpose, uses, warnings, do not use, when using this product, stop use and ask a doctor, keep out of the reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
AVOBENZONE 3.0%, HOMOSALATE 15.0%, OCTISALATE 5.0%, OCTOCRYLENE 2.8%,
OXYBENZONE 6.0%
Sunscreen
For external use only
on damaged or broken skin
keep out of eyes. Rinse with water to remove.
if rash occurs
If product is swallowed, get medical help or contact a Poison Control Center right away.
Water, Styrene/Acrylates Copolymer, Butyloctyl Salicylate, Silica, Glyceryl Stearate, PEG-100 Stearate, Caprylyl Methicone, Sodium Polyacrylate, Benzyl Alcohol, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Ethylhexyl Stearate, Beeswax, Dimethicone, Chlorphenesin, Cetyl Dimethicone, Xanthan Gum, Trimethylsiloxysilicate, Fragrance, Trideceth-6, Disodium EDTA, BHT, Dipotassium Glycyrrhizate.
* Please review the disclaimer below.