NU SKIN SUNRIGHT 35 BROAD SPECTRUM SPF 35- titanium dioxide and zinc oxide lotion

Nu Skin Sunright 35 Broad Spectrum SPF 35 by

Drug Labeling and Warnings

Nu Skin Sunright 35 Broad Spectrum SPF 35 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

Titanium Dioxide 4.2%, Zinc Oxide 4.5%.

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/Dimethicone Copolymer, C12-15 Alkyl Benzoate, Allantoin, Aloe Barbadensis Leaf Juice, Bisabolol, Caprylic/Capric Triglyceride, Caprylyl Methicone, Carthamus Tinctorius (Safflower) Seed Oil, Chlorphenesin, Cyclopentasiloxane, Di-C12-13 Alkyl Tartrate, Dicaprylyl Carbonate, Diglycerin, Dimethicone/PEG-10/15 Crosspolymer, Dimethicone/Vinyl Dimethicone Crosspolymer, Fragrance (Parfum), Haematococcus Pluvialis Extract, Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone, Panthenol, Phenoxyethanol, Physalis Angulata Extract, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Propylene Carbonate, Propylheptyl Caprylate, Silica, Sodium Chloride, Sodium Citrate, Stearalkonium Hectorite, Tocopherol, Triethoxysilylethyl Polydimethylsiloxyethyl Hexyl Dimethicone, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Water (Aqua).

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® 35

BROAD SPECTRUM
SPF 35

Face & Body
Sunscreen

Water Resistant
(80 minutes)

100 ml e (3.4 fl. oz.)

INGREDIENTS AND APPEARANCE

NU SKIN SUNRIGHT 35 BROAD SPECTRUM SPF 35 
titanium dioxide and zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 62839-1344
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP)	Titanium Dioxide	42 mg  in 1 mL
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z)	Zinc Oxide	45 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
Alkyl (C12-15) Benzoate (UNII: A9EJ3J61HQ)
Allantoin (UNII: 344S277G0Z)
Aloe Vera Leaf (UNII: ZY81Z83H0X)
Levomenol (UNII: 24WE03BX2T)
Medium-Chain Triglycerides (UNII: C9H2L21V7U)
Caprylyl Trisiloxane (UNII: Q95M2P1KJL)
Safflower Oil (UNII: 65UEH262IS)
Chlorphenesin (UNII: I670DAL4SZ)
Cyclomethicone 5 (UNII: 0THT5PCI0R)
Di-C12-13 Alkyl Tartrate (UNII: 603USX4K0G)
Dicaprylyl Carbonate (UNII: 609A3V1SUA)
Diglycerin (UNII: 3YC120743U)
Dimethicone (UNII: 92RU3N3Y1O)
Haematococcus Pluvialis (UNII: 31T0FF0472)
Lauryl PEG-9 Polydimethylsiloxyethyl Dimethicone (UNII: 25G622K2RA)
Panthenol (UNII: WV9CM0O67Z)
Phenoxyethanol (UNII: HIE492ZZ3T)
Physalis Angulata (UNII: W4TKW9D5GG)
Propylene Carbonate (UNII: 8D08K3S51E)
Propylheptyl Caprylate (UNII: 991Z19V2OD)
Silicon Dioxide (UNII: ETJ7Z6XBU4)
Sodium Chloride (UNII: 451W47IQ8X)
Sodium Citrate, Unspecified Form (UNII: 1Q73Q2JULR)
Stearalkonium Hectorite (UNII: OLX698AH5P)
Tocopherol (UNII: R0ZB2556P8)
Water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 62839-1344-1	1 in 1 CARTON	04/23/2014
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	04/23/2014

Labeler - NSE Products, Inc. (803486393)