Other
Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Cardon, Inc for the product Cardon (NDC 72475-001). 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, otc - active ingredient, otc - purpose, indications & usage, 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
Active ingredients
Homosalate 7%
Ethylhexyl salicylate 4.3%
Butyl methoxydibenzoylmethane 2.5%
Purpose
sunscreen
Uses
Warnings
Directions
Other information
Other information
Inactive ingredients water, propanediol, butyloctyl salicylate, ethylhexyl methoxycrylene, polymethyl methacrylate, butylene glycol, 1,2-hexanediol, styrene/acrylates copolymer, phenoxyethanol, fragrance, glycerin, pentylene glycol, saccharide hydrolysate, sodium acrylate/sodiumacryloyldimethyl taurate copolymer, carbomer, polyacrylate crosspolymer-6, behenyl alcohol, ethylhexyglycerin, hydroxyethyl acrylate/sodiumacryloyldimethyl taurate copolymer, tromethamine, xanthan gum, isohexadecane, curcuma longa (turmeric) root extract, portulaca oleracea extract, centella asiatica extract, houttuynia cordata extract, salvia hispanica seed extract, opuntia ficus-indica stem extract, t-butyl alcohol, disodium edta, oxygen
CARDON
SPF + MOISTURIZER
BROAD SPECTRUM SPF 30
1.2 FL.OZ. / 35 ml
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