SeneSun

Manufacturer
SGII, INC.
Effective date
2018-11-17
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 00:45:49

Label at a glance#

ProductSeneSun
Active ingredientOCTINOXATE, HOMOSALATE, OXYBENZONE, OCTISALATE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Ethylhexyl Methoxycinnamate    7.5%

Homosalate    6.0%

Benzophenone-3    6.0%

Ethylhexyl Salicylate    5.0%

OTC - PURPOSE SECTION

Purpose

Sunscreen

INDICATIONS & USAGE SECTION

Uses: Helps prevent sunburn

WARNINGS SECTION

Warnings: For external use only.

OTC - WHEN USING SECTION

When using this product:

keep out of eyes. Rinse with water to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get  medical help or contact a Poison Control Center right away.

INSTRUCTIONS FOR USE SECTION

Directions:

For sunscreen use: spray evenly and spread evenly by hand 15 minutes before sun exposure. Apply to all skin exposed to sun. Hold container 4 to 6 inches from the skin to apply. Do not spray directly into face. Spray on hands, then apply to face. Do not apply in windy conditions. 

DOSAGE & ADMINISTRATION SECTION

 Children under 6 months of age: ask a doctor.

OTC - DO NOT USE SECTION

Stop use and ask a doctor if:

if rash occurs.

INACTIVE INGREDIENT SECTION

Water (Aqua Purificata) Purified, C12-15 Alkyl Benzoate, Polysorbate 20, Aloe Barbadensis Leaf Juice, Orchid Extract, Algae Extract, Glucosamine HCL, Yeast Extract, Tocopherol, Tocopheryl Acetate, Retinyl Palmitate, Dimethicone, Sodium PCA, Ethylhexyl Palmitate, Tricontanyl PVP, Acrylates/C10-30 Alkyl Acrylates Crosspolymer, Tetrasodium EDTA, Urea, Triethanolamine, Phenoxyethanol, Methylparaben, Ethylparaben, Butylparaben, Propylparaben, Isobutylparaben, Fragrance (Parfum).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SENESUNSENESUN

Products#

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DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72644-62772644-627-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 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
8e09d3e6-40fd-4fd4-a1e9-623c71cf3c9dc17db4fd-ab0c-4d90-88b5-abbaa71f25bb2018-11-17WarningsExact identifier
spl id: 8e09d3e6-40fd-4fd4-a1e9-623c71cf3c9d
spl set id: c17db4fd-ab0c-4d90-88b5-abbaa71f25bb

Reported adverse events (FAERS/openFDA)#

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