Neova Day Therapy

Manufacturer
PHARMA COSMETICS, INC | Northwest Cosmetic Laboratories LLC
Effective date
2022-10-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:50:55

Label at a glance#

ProductNeova Day Therapy SPF 30
Active ingredientHOMOSALATE, OCTOCRYLENE, OCTISALATE, AVOBENZONE
Label structure5 sections

Indications and uses

helps in prevents sunburn If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun. • Apply liberally 15 minutes before sun exposure. • Use a water resistant sunscreen if swimming or sweating. • Reapply at least every 2 hours. • Children under 6 months of age: ask a doctor. • Sun Protection Measures. Spending time in the sun i...

Label contents#

Full prescribing information#

Warnings

WARNINGS AND PRECAUTIONS SECTION

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.

USES

INTENDED USE OF THE DEVICE

  • helps in prevents sunburn
  • If used as directed with other sun protection measures
    (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

Directions

INDICATIONS & USAGE SECTION

• Apply liberally 15 minutes before sun exposure.
• Use a water resistant sunscreen if swimming or sweating.
• Reapply at least every 2 hours.
• Children under 6 months of age: ask a doctor.
• Sun Protection Measures. Spending time in the sun increases your risk of skin
cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad
spectrum SPF of 15 or higher and other sun protection measures including:
• Limit time in the sun, especially from 10 a.m. – 2 p.m.
• Wear long-sleeve shirts, pants, hats, and sunglasses

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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) Kernel Oil, Squalane,
Ammonium Acrylate/Acrylamide Copolymer, Polyisobutene, Polysorbate
20, Sodium Hydroxide, Lecithin, Sodium Chloride, Phenoxyethanol, Sorbic
Acid. May Contain +/- Ultramarines.

Product Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72251-00472251-004-50

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 30 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ebde006c-cc64-8eb5-e053-2995a90a98e49634372c-d402-49b7-9232-3cddd5ba2b0f2022-10-25WarningsExact identifier
spl id: ebde006c-cc64-8eb5-e053-2995a90a98e4
spl set id: 9634372c-d402-49b7-9232-3cddd5ba2b0f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.