FDA.reportPublic FDA data

Sunright

Manufacturer
NSE Products, Inc.
Effective date
2026-04-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:53:26

Label at a glance#

ProductSunright 50
Active ingredientAvobenzone, Homosalate, Octinoxate
Label structure9 sections

Indications and uses

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.

Dosage and administration

Apply liberally 15 minutes before sun or water exposure. Reapply: After 80 minutes of swimming or sweating Immediately after towel drying At least every 2 hours Children under 6 months: Ask a doctor

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%, Homosalate 15.0%, Octisalate 5.0%.

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • 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.

Warning

WARNINGS SECTION

  • For external use only. Do not use on broken or damaged skin. Stop use and ask a doctor if rash occurs. When using this product, keep out of eyes. Rinse with water to remove.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply liberally 15 minutes before sun or water exposure.
  • Reapply: After 80 minutes of swimming or sweating
    • Immediately after towel drying
    • At least every 2 hours
  • Children under 6 months: Ask a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Aloe Barbadensis Leaf Juice, Acrylates Copolymer, Butyloctyl Salicylate, Propanediol, Caprylyl Methicone, Pentylene Glycol, Triacontanyl PVP, Potassium Cetyl Phosphate, Haematococcus Pluvialis Extract, Physalis Angulata Extract, Allantoin, Bisabolol, Panthenol, Tocopherol, Caprylic/Capric Triglyceride, VP/Acrylates/Lauryl Methacrylate Copolymer, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Acrylic Acid/VP Crosspolymer, Fragrance (Parfum), Hydroxyacetophenone, Sodium Dehydroacetate, Aminomethyl Propanol, Disodium EDTA.

Questions?

OTC - QUESTIONS SECTION

1-800-487-1000

PRINCIPAL DISPLAY PANEL - 100 mL Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NU SKIN®

SUNRIGHT® 50

BROAD SPECTRUM
SPF 50

FACE & BODY SUNSCREEN
WATER RESISTANT 80 MINUTES

100 mL ℮ 3.4 Fl Oz

PRINCIPAL DISPLAY PANEL - 100 mL Tube Label
PRINCIPAL DISPLAY PANEL - 100 mL Tube Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62839-2011-1Sunright 50100 mL in 1 TUBELOTION1001

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62839-201162839-2011-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
AvobenzoneG63QQF2NOXACTIB
HomosalateV06SV4M95SACTIB
Octinoxate4Y5P7MUD51ACTIB
Water059QF0KO0RIACT
ALOE VERA LEAF JUICERUE8E6T4NBIACT
Butyloctyl Salicylate2EH13UN8D3IACT
Propanediol5965N8W85TIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
Pentylene Glycol50C1307PZGIACT
TRICONTANYL POVIDONEN0SS3Q238DIACT
Potassium Cetyl Phosphate03KCY6P7UTIACT
HydroxyacetophenoneG1L3HT4CMHIACT
Sodium Dehydroacetate8W46YN971GIACT
AMINOMETHYLPROPANOLLU49E6626QIACT
PHYSALIS ANGULATA WHOLEW4TKW9D5GGIACT
LEVOMENOL24WE03BX2TIACT
EDETATE DISODIUM7FLD91C86KIACT
Allantoin344S277G0ZIACT
PanthenolWV9CM0O67ZIACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
HAEMATOCOCCUS PLUVIALIS31T0FF0472IACT
TocopherolR0ZB2556P8IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sunright 50AVOBENZONE, HOMOSALATE, AND OCTINOXATENSE Products, Inc.b1b76481-da23-427f-9b34-b987019fa5322026-04-09WarningsExact identifier
ndc (package): 62839-2011-1
ndc (product): 62839-2011
ndc11 (package): 62839201101
spl id: b43a24fc-7faa-4721-9f72-7fc5b4fd857c
spl set id: b1b76481-da23-427f-9b34-b987019fa532

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.