SUNRIGHT BODYBLOCK SPF15- avobenzone, octinoxate, octisalate, and oxybenzone lotion

Sunright BodyBlock SPF15 by

Drug Labeling and Warnings

Sunright BodyBlock SPF15 by is a Otc medication manufactured, distributed, or labeled by NSE Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Avobenzone 2%, Octinoxate 7.5%, Octisalate 3%, Oxybenzone 3%.

Warnings

For external use only.

Not to be swallowed. Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Discontinue use if rash or irritation appear. If irritation or rash persists, consult a doctor.

Keep out of reach of children.

Directions

Adults and children 6 months of age and over: Apply evenly 30 minutes before sun or water exposure. Reapply after swimming or excessive perspiring or anytime after towel drying. Children under 2 years of age: Use sunscreen products with a minimum SPF of 4. Children under 6 months of age: consult a doctor. Note: As with similar products, avoid immediate contact with natural fibers upon application.

Inactive Ingredients

Water (Aqua), Octyldodecyl Neopentanoate, Butylene Glycol, Glycerin, Aluminum Starch Octenylsuccinate, Tricontanyl PVP, Chlorella Vulgaris Extract,1 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 (Parfum), Propylparaben, Phenoxyethanol, Chlorphenesin, Methylparaben, Ethylparaben, Benzyl Alcohol.

1 SeaLastin

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 100 ml Carton

SUNRIGHT®

with SeaLastin

BodyBlock
SPF 15

Face & Body Sunscreen
Water Resistant

100 ml e (3.4 fl. oz.)

INGREDIENTS AND APPEARANCE

SUNRIGHT BODYBLOCK SPF15 
avobenzone, octinoxate, octisalate, and oxybenzone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1133
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX)	Avobenzone	20 g  in 1000 mL
Octinoxate (UNII: 4Y5P7MUD51) (Octinoxate - UNII:4Y5P7MUD51)	Octinoxate	75 g  in 1000 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W)	Octisalate	30 g  in 1000 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y)	Oxybenzone	30 g  in 1000 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: 62839-1133-1	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. (966817975)