NU SKIN SUNRIGHT 35 BROAD SPECTRUM SPF 35- titanium dioxide and zinc oxide lotion 
NSE Products, Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Nu Skin® Sunright® 35 Broad Spectrum SPF 35

Drug Facts

Active Ingredient

Titanium Dioxide 4.2%, Zinc Oxide 4.5%.

Purpose

Sunscreen

Use

Warnings

  • 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

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

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.)

Principal Display Panel - 100 mL Bottle Carton
NU SKIN SUNRIGHT 35 BROAD SPECTRUM SPF 35 
titanium dioxide and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62839-1344
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Titanium Dioxide (UNII: 15FIX9V2JP) (Titanium Dioxide - UNII:15FIX9V2JP) Titanium Dioxide42 mg  in 1 mL
Zinc Oxide (UNII: SOI2LOH54Z) (Zinc Oxide - UNII:SOI2LOH54Z) Zinc Oxide45 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 whole (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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:62839-1344-11 in 1 CARTON04/23/2014
1100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35204/23/2014
Labeler - NSE Products, Inc. (803486393)

Revised: 1/2022
Document Id: 64b34bac-87cc-4849-aa41-f6c400f96ff9
Set id: 11d83621-2abb-49bc-bdc6-887d450c753e
Version: 3
Effective Time: 20220114
 
NSE Products, Inc.