NU SKIN SUNRIGHT 50 BROAD SPECTRUM SPF 50- avobenzone, homosalate, octinoxate, octisalate, and octocrylene lotion

Nu Skin Sunright 50 Broad Spectrum SPF 50 by

Drug Labeling and Warnings

Nu Skin Sunright 50 Broad Spectrum SPF 50 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%, Homosalate 10.0%, Octinoxate 7.5%, Octisalate 5%, Octocrylene 6.5%.

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

Acrylates Copolymer, Allantoin, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Bisabolol, Butylene Glycol, Caprylic/Capric Triglyceride, Carbomer, Caprylyl Glycol, Carthamus Tinctorius (Safflower) Seed Oil, Cetyl Alcohol, Chlorphenesin, Cyclohexasiloxane, Cyclopentasiloxane, Dimethicone/Vinyl Dimethicone Crosspolymer, Dimethicone/Vinyltrimethylsiloxysilicate Crosspolymer, Disodium EDTA, Fragrance (Parfum), Glyceryl Stearate, Haematococcus Pluvialis Extract, 1,2-Hexanediol, Panthenol, PEG-100 Stearate, Phenoxyethanol, Physalis Angulata Extract, Polyacrylate-13, Polyisobutene, Polysorbate 20, Steareth-2, Steareth-21, Titanium Dioxide, Tocopherol, Water (Aqua), Xanthan Gum.

Other Information

• Protect this product from excessive heat and direct sun.

Questions?

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Carton

NU SKIN®

SUNRIGHT® 50

BROAD SPECTRUM
SPF 50

Face & Body
Sunscreen

Water Resistant
(80 minutes)

100 ml e (3.4 fl. oz.)

INGREDIENTS AND APPEARANCE

NU SKIN SUNRIGHT 50 BROAD SPECTRUM SPF 50 
avobenzone, homosalate, octinoxate, octisalate, and octocrylene lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1345
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
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S)	Homosalate	100 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
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM)	Octocrylene	65 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Allantoin (UNII: 344S277G0Z)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Aminomethylpropanol (UNII: LU49E6626Q)
Levomenol (UNII: 24WE03BX2T)
Butylene Glycol (UNII: 3XUS85K0RA)
Medium-Chain Triglycerides (UNII: C9H2L21V7U)
Caprylyl Glycol (UNII: 00YIU5438U)
Safflower Oil (UNII: 65UEH262IS)
Cetyl Alcohol (UNII: 936JST6JCN)
Chlorphenesin (UNII: I670DAL4SZ)
Cyclomethicone 6 (UNII: XHK3U310BA)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Edetate Disodium (UNII: 7FLD91C86K)
Glyceryl Monostearate (UNII: 230OU9XXE4)
Haematococcus Pluvialis (UNII: 31T0FF0472)
1,2-Hexanediol (UNII: TR046Y3K1G)
Panthenol (UNII: WV9CM0O67Z)
PEG-100 Stearate (UNII: YD01N1999R)
Phenoxyethanol (UNII: HIE492ZZ3T)
Physalis Angulata (UNII: W4TKW9D5GG)
Steareth-2 (UNII: V56DFE46J5)
Steareth-21 (UNII: 53J3F32P58)
Polysorbate 20 (UNII: 7T1F30V5YH)
Titanium Dioxide (UNII: 15FIX9V2JP)
Tocopherol (UNII: R0ZB2556P8)
Water (UNII: 059QF0KO0R)
Xanthan Gum (UNII: TTV12P4NEE)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-1345-1	1 in 1 CARTON	06/02/2014
1		100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH FINAL	part352	06/02/2014

Labeler - NSE Products, Inc. (803486393)