Directions For Use:
Apply liberally to exposed skin every two hours. Reapply as needed. For optimal results, use daily with Neova [DNA + Copper] products.
Neova Dna Damage Control - Active
FDA Label NDC 62362-129
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Photomedex, Inc. for the product Neova Dna Damage Control - Active (NDC 62362-129). 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 directions for use:, supplied, active ingredients:, inactive ingredients:, image of package, pouch, and package insert, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Supplied
in a 3.0 fl. oz. / 89 mL tube.
Active Ingredients:
Zinc Oxide 8.0%, Octinoxate 7.5%, Octisalate 3.0%.
Inactive Ingredients:
Water (Aqua), Cyclopentasiloxane,
Ethyl Hexyl Isononanoate, Micrococcus Lysate, Plankton
Extract, L-ergothioneine, Dimethicone, Dimethicone/
PEG-10/15 Crosspolymer, Lauryl PEG-9 Polymethylsiloxyethyl
Dimethicone, Dimethicone/Vinyl Dimethicone
Crosspolymer, Retinyl Palmitate, Ascorbyl Palmitate
(Vitamin C), Sodium Chloride, Phenoxyethanol, Butylene
Glycol, Iodopropynyl Butylcarbamate, Citric Acid,
Sodium Hydroxide.
Image Of Package, Pouch, And Package Insert
AmpuleActive.jpg
Package (Ampuleactive)
Pouch (Pouchactive)
Package Insert Page 1 (Pkginsertuniversalpg1)
Package Insert Page 2 (Pkginsertuniversalpg2)
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