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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Dermalogica, Inc. for the product Daily Defense (NDC 68479-800). 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 other, active ingredients, purpose, uses, warnings, otc - do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Avobenzone (3.0%), Octinoxate (6.5%), Octisalate (3.0%), Oxybenzone (3.5%).
Sunscreen
For external use only
Do not use on damaged 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 right away.
Water/Aqua/Eau, Butylene Glycol, Caprylic/Capric Triglyceride, Glyceryl Stearate, Cetearyl Phosphate, Glycerin, Stearic Acid, Polyglyceryl-2 Stearate, Dimethicone, Lactamide MEA, Pyrus Malus (Apple) Fruit Extract, Dimethyl Capramide, Mahonia Aquifolium Root Extract, Lavandula Angustifolia (Lavender) Extract, Hydrolyzed Opuntia Ficus Indica Flower Extract, Triticum Vulgare (Wheat) Germ Extract, Saccharomyces Cerevisiae Extract, Lavandula Spica (Lavender) Flower Oil, Lavandula Hybrida Oil, Eucalyptus Globulus Leaf Oil, Sodium Hyaluronate, Dipotassium Glycyrrhizate, Palmitoyl Tripeptide-5, Sodium DNA, Tocopherol, Allantoin, Panthenol, Glycerin Crosspolymer, Ascorbyl Tetraisopalmitate, Carbomer, Polyquaternium-10, Cetyl Alcohol, Xanthan Gum, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Disodium EDTA, Citric Acid, Potassium Sorbate, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol.
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