SENESUN- sunscreen spray

SeneSun by

Drug Labeling and Warnings

SeneSun by is a Otc medication manufactured, distributed, or labeled by SGII, INC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Ethylhexyl Methoxycinnamate    7.5%

Homosalate    6.0%

Benzophenone-3    6.0%

Ethylhexyl Salicylate    5.0%

PURPOSE

Purpose

Sunscreen

INDICATIONS & USAGE

Uses: Helps prevent sunburn

WARNINGS

Warnings: For external use only.

WHEN USING

When using this product:

keep out of eyes. Rinse with water to remove.

KEEP OUT OF REACH OF CHILDREN

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

INSTRUCTIONS FOR USE

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

 Children under 6 months of age: ask a doctor.

DO NOT USE

Stop use and ask a doctor if:

if rash occurs.

INACTIVE INGREDIENT

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).

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SENESUN 
sunscreen spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72644-627
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7.5 mg  in 1 mg
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	6 mg  in 1 mg
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y)	OXYBENZONE	6 mg  in 1 mg
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	5 mg  in 1 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
YEAST (UNII: 3NY3SM6B8U)
TOCOPHEROL (UNII: R0ZB2556P8)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
DIMETHICONE (UNII: 92RU3N3Y1O)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
TRICONTANYL POVIDONE (UNII: N0SS3Q238D)
CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L)
EDETATE SODIUM (UNII: MP1J8420LU)
UREA (UNII: 8W8T17847W)
TROLAMINE (UNII: 9O3K93S3TK)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
METHYLPARABEN (UNII: A2I8C7HI9T)
ETHYLPARABEN (UNII: 14255EXE39)
BUTYLPARABEN (UNII: 3QPI1U3FV8)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
ISOBUTYLPARABEN (UNII: 0QQJ25X58G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72644-627-12	120 mg in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	06/29/2018	09/30/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	06/29/2018	09/30/2020

Labeler - SGII, INC. (070096792)