Neova Day Therapy
FDA Label NDC 62362-184

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 Day Therapy (NDC 62362-184). 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 warnings:, directions:, supplied, active ingredients:, purpose:, ingredients:, image of packet, packet holder, package insert, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Warnings:

→ Directions:

→ Supplied

→ Active Ingredients:

→ Purpose:

→ Ingredients:

→ Image Of Packet, Packet Holder, Package Insert

Warnings:

For external use only. Avoid contact
with eyes. If contact occurs, rinse eyes thoroughly
with water. Discontinue use if irritation or rash appears.
Keep out of reach of children. In case of accidental
ingestion, seek professional assistance or contact
a Poison Control Center immediately.

Directions:

Apply liberally to face and neck in the morning.

Supplied

in a 1.7 oz / 50mL airless pump.

Active Ingredients:

Homosalate 7%, Octocrylene, 6%,
Octisalate 5%, Avobenzone 3%

Purpose:

Sunscreen

Ingredients:

Water (Aqua), Isododecane, Hydrogenated
Polydecene, Glycerin, Glyceryl Stearate, Arachidyl
Alcohol, Behenyl Alcohol, Bis (Tripeptide-1) Copper
Acetate, Plankton Extract, Triticum Vulgare (Wheat)
Gluten Extract, Glycine Soja (Soybean) Seed Extract,
Dimethicone, Arachidyl Glucoside, Caprylyl Glycol,
Xanthan Gum, Cetyl Alcohol, PEG-100 Stearate, Prunus
Armeniaca (Apricot) Kernal Oil, Squalane, Ammonium
Acrylate/Acrylamide Copolymer, Polyisobutene, Polysorbate
20, Sodium Hydroxide, Lecithin, Sodium
Chloride, Phenoxyethanol, Sorbic Acid. May Contain
+/- Ultramarines.