Otc - Active Ingredient
ACTIVE INGREDIENT -
Benzophenone 3.6%
Avobenzone 1%
Octinoxate 7.5%
Octisalate 5%
Complexion Protection Moisturizer Spf
FDA Label NDC 70809-1902
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Usrx Llc for the product Complexion Protection Moisturizer Spf (NDC 70809-1902). 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 package label.principal display panel, otc - active ingredient, otc - purpose, warnings, otc - do not use, otc - stop use, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Sunscreen
Warnings
FOR EXTERNAL USE ONLY
Otc - Do Not Use
DO NOT USE - On damaged or broken skin
Otc - Stop Use
STOP USE AND ASK A DOCTOR IF A RASH OCCURRS
Inactive Ingredient
Aqua (Water), Caprylic/Capric Triglyceride, Corn Starch Modified, Cetearyl Olivate, Diethylhexyl 2,6-Naphthalate, C12-15 Alkyl Benzoate, Sorbitan Olivate, Gluconolactone, Squalane, Glycerin, Cyclopentasiloxane, Tocopheryl Acetate (D-alpha), Sodium Hyaluronate (L), Xanthan Gum, Carbomer, Aminomethyl Propanol, Sodium Benzoate, Phenethyl Alcohol, Caprylyl Glycol, Phenoxyethanol, Trisodium Ethylenediamine Disuccinate, Potassium Sorbate
* Please review the disclaimer below.
