FDA.reportPublic FDA data

Sunright

Manufacturer
NSE Products, Inc.
Effective date
2026-04-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:53:27

Label at a glance#

ProductSunright Lip Balm
Active ingredientOctinoxate, Avobenzone, Octocrylene
Label structure10 sections

Dosage and administration

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

Storage and handling

Protect this product from excessive heat and direct sun. Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun. 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...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 3.0%, Octinoxate 7.5%, Octocrylene 2.79%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Use

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn.
  • Higher SPF gives more sunburn protection.

Warnings

WARNINGS SECTION

  • For external use only.

OTC - DO NOT USE SECTION

  • Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

  • When using this product keep out of eyes. Rinse with water to remove.

OTC - STOP USE SECTION

  • Stop use and ask a doctor if rash occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Ricinus Communis (Castor) Seed Oil, Helianthus Annuus (Sunflower) Seed Oil, Beeswax, Euphorbia Cerifera (Candelilla) Wax, Ozokerite, Polyethylene, Caprylic/Capric Triglyceride, Octyldodecyl Neopentanoate, Flavor (Aroma), Silica, Glycine Soja (Soybean) Germ Extract, Zea Mays (Corn) Starch, Ethyl Vanillin, Chlorella Vulgaris Extract, Tocopheryl Acetate, Water (Aqua), Ethylhexylglycerin, Phenoxyethanol.

Other Information

STORAGE AND HANDLING SECTION

  • Protect this product from excessive heat and direct sun.
  • Sun alert: Limiting sun exposure, wearing protective clothing, and using sunscreens may reduce the risks of skin aging, skin cancer, and other harmful effects of the sun.
  • 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.–2 p.m.
    • Wear long-sleeved shirts, pants, hats, and sunglasses.

Questions?

OTC - QUESTIONS SECTION

1-801-345-9900

PRINCIPAL DISPLAY PANEL - 4.2 g Tube Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NU SKIN®

SUNRIGHT® LIP BALM

BROAD SPECTRUM

SPF 15

4.2 g

Principal Display Panel - 4.2 g Tube Carton
Principal Display Panel - 4.2 g Tube Carton

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62839-2918-1Sunright Lip Balm1 in 1 CARTONSTICK11
62839-2918-1Sunright Lip Balm4.2 g in 1 TUBESTICK4.21

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62839-291862839-2918-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
Octinoxate4Y5P7MUD51ACTIB
AvobenzoneG63QQF2NOXACTIB
Octocrylene5A68WGF6WMACTIB
CASTOR OILD5340Y2I9GIACT
SUNFLOWER OIL3W1JG795YIIACT
CANDELILLA WAXWL0328HX19IACT
YELLOW WAX2ZA36H0S2VIACT
CERESINQ1LS2UJO3AIACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
MEDIUM-CHAIN TRIGLYCERIDESC9H2L21V7UIACT
OCTYLDODECYL NEOPENTANOATEX8725R883TIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
SOYBEAN GERMJBW2VHD14MIACT
STARCH, CORNO8232NY3SJIACT
ETHYL VANILLINYC9ST449YJIACT
PHENOXYETHANOLHIE492ZZ3TIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
WATER059QF0KO0RIACT
CHLORELLA VULGARISRYQ4R60M02IACT

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 Lip BalmOCTINOXATE, AVOBENZONE, AND OCTOCRYLENENSE Products, Inc.dfdb2d0a-c646-4c44-b648-e2fdd604cdc92026-04-08WarningsExact identifier
ndc (package): 62839-2918-1
ndc (product): 62839-2918
ndc11 (package): 62839291801
spl id: 574025e1-5166-4ba3-adf3-529291e81648
spl set id: dfdb2d0a-c646-4c44-b648-e2fdd604cdc9

Reported adverse events (FAERS/openFDA)#

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