Otc - Active Ingredient
ACTIVE INGREDIENT: OCTINOXATE 5.40%
Virtual Skin
FDA Label NDC 59158-759
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Prescriptives Inc. for the product Virtual Skin (NDC 59158-759). 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, inactive ingredient, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
INACTIVE INGREDIENTS: WATER\AQUA\EAU [] DIMETHICONE [] CYCLOPENTASILOXANE [] GLYCERYL STEARATE SE [] HDI/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER [] BUTYLENE GLYCOL [] TALC [] CHOLESTEROL [] TRITICUM VULGARE (WHEAT BRAN) EXTRACT [] MELANIN [] SODIUM HYALURONATE [] TOCOPHERYL ACETATE [] OLEA EUROPAEA (OLIVE) FRUIT EXTRACT [] POLYACRYLAMIDE [] ETHYLHEXYLGLYCERIN [] PALMITIC ACID [] C13-14 ISOPARAFFIN [] CAPRYLYL GLYCOL [] LAURETH-7 [] HEXYLENE GLYCOL [] LINOLEIC ACID [] PEG-9 DIMETHICONE [] SILICA [] CITRIC ACID [] SODIUM CITRATE [] DISODIUM EDTA [] SORBIC ACID [] BENZOIC ACID [] POTASSIUM SORBATE [] PHENOXYETHANOL [] [+/- TITANIUM DIOXIDE (CI 77891) [] IRON OXIDES (CI 77491, CI 77492, CI 77499) [] MICA
Warnings
WARNINGS: FOR EXTERNAL USE ONLY. KEEP OUT OF EYES. RINSE WITH WATER TO REMOVE. STOP USE AND ASK A DOCTOR IF SKIN RASH OR IRRITATION OCCURS. KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.
Package Label.Principal Display Panel
PRESCRIPTIVES
VIRTUAL SKIN
SUPER NATURAL FINISH
SPF 10
1.0 FL OZ LIQ/ 30 ML
PRESCRIPTIVES CO. DIST
NY NY 10022
Folding Carton (9716)
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