SUNRIGHT BROAD SPECTRUM SPF 30- avobenzone, octinoxate, octisalate, and oxybenzone lotion

Sunright Broad Spectrum SPF 30 by

Drug Labeling and Warnings

Sunright Broad Spectrum SPF 30 by is a Otc medication manufactured, distributed, or labeled by NSE Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

Avobenzone 3.0%, Octinoxate 7.5%, Octisalate 5%, Oxybenzone 5%.

Purpose

Sunscreen

Use

• Helps prevent sunburn. Higher SPF gives more sunburn protection.
• 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.

Warnings

• For external use only.

• Do not use on damaged or broken skin

• Stop use and ask a doctor if rash occurs

• When using this product, keep out of eyes. Rinse with water to remove.

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

Directions

• Apply liberally 15 minutes before sun exposure.
• Reapply:
  • After 40 minutes of swimming or sweating
  • Immediately after towel drying
  • At least every 2 hours
• Children under 6 months: Ask a doctor
• Sunprotection 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.–2p.m.
  • Wear long-sleeved shirts, pants, hats, and sunglasses.

Inactive Ingredients

Water, Octyldodecyl Neopentanoate, Butylene Glycol, Glycerin, Aluminum Starch Octenylsuccinate, Triacontanyl PVP, Chlorella Vulgaris Extract, Tocopheryl Acetate, Tetrahexyldecyl Ascorbate, Stearyl Glycyrrhetinate, PEG-20 Almond Glycerides, Hydrogenated Castor Oil, Boron Nitride, Xanthan Gum, Silica Dimethyl Silylate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Cetyl Alcohol, Stearic Acid, Carbomer, Tetrasodium EDTA, Aminomethyl Propanol, Fragrance, Phenoxyethanol, Chlorphenesin, Methylparaben, Propylparaben, Ethylparaben, Benzyl Alcohol.

Other Information

• Protect this product from excessive heat and direct sun.

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 100 ml Tube Carton

SUNRIGHT®

with SeaLastin

BROAD SPECTRUM
SPF 30

Face & Body Sunscreen
Water Resistant (40 Minutes)

100 ml e (3.4 FL. OZ.)

INGREDIENTS AND APPEARANCE

SUNRIGHT BROAD SPECTRUM SPF 30 
avobenzone, octinoxate, octisalate, and oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1332
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	30 mg  in 1 mL
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	50 mg  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y)	Oxybenzone	50 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Water (UNII: 059QF0KO0R)
Octyldodecyl Neopentanoate (UNII: X8725R883T)
Butylene Glycol (UNII: 3XUS85K0RA)
Glycerin (UNII: PDC6A3C0OX)
Aluminum Starch Octenylsuccinate (UNII: I9PJ0O6294)
Chlorella Vulgaris (UNII: RYQ4R60M02)
Tetrahexyldecyl Ascorbate (UNII: 9LBV3F07AZ)
Hydrogenated Castor Oil (UNII: ZF94AP8MEY)
Boron Nitride (UNII: 2U4T60A6YD)
Xanthan Gum (UNII: TTV12P4NEE)
Cetyl Alcohol (UNII: 936JST6JCN)
Stearic Acid (UNII: 4ELV7Z65AP)
Edetate Sodium (UNII: MP1J8420LU)
Aminomethylpropanol (UNII: LU49E6626Q)
Propylparaben (UNII: Z8IX2SC1OH)
Phenoxyethanol (UNII: HIE492ZZ3T)
Chlorphenesin (UNII: I670DAL4SZ)
Methylparaben (UNII: A2I8C7HI9T)
Ethylparaben (UNII: 14255EXE39)
Benzyl Alcohol (UNII: LKG8494WBH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-1332-1	1 in 1 CARTON
1		100 mL in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part352	09/01/2010

Labeler - NSE Products, Inc. (803486393)