Nu Skin

Manufacturer
NSE Products, Inc
Effective date
2026-04-06
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:52:41

Label at a glance#

ProductNu Skin Sunright Lip Balm Broad Spectrum SPF 15
Active ingredientOCTINOXATE, AVOBENZONE, OCTOCRYLENE
Label structure10 sections

Dosage and administration

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. Apply liberally 15 minutes before sun exposure. Reapply at least e...

Storage and handling

Protect this product from excessive heat and direct sun.

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.
  • 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

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

  • 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.
  • Apply liberally 15 minutes before sun exposure.
  • Reapply at least every two hours.
  • Use a water resistant sunscreen if swimming or sweating.
  • 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), Glycine Soja (Soybean) Oil, Ethyl Vanillin, Chlorella Vulgaris Extract, Tocopherol, Tocopheryl Acetate, Zea Mays (Corn) Starch, Silica, Water (Aqua), Ethylhexylglycerin, Phenoxyethanol.

Other Information

STORAGE AND HANDLING SECTION

  • Protect this product from excessive heat and direct sun.

Questions?

OTC - QUESTIONS SECTION

1-888-742-7626

PRINCIPAL DISPLAY PANEL - 15 ml Tube Pouch Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NU SKIN®

SUNRIGHT®
Lip Balm
BROAD SPECTRUM SPF 15

15 ml e (0.5 fl. oz.)

PRINCIPAL DISPLAY PANEL - 15 ml Tube Pouch Label
PRINCIPAL DISPLAY PANEL - 15 ml Tube Pouch Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
baf7f49c-75b6-496b-a00e-8e766a8e4f03Product name120210127
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62839-6201-1Nu Skin Sunright Lip Balm Broad Spectrum SPF 151 in 1 POUCHSTICK14
62839-6201-1Nu Skin Sunright Lip Balm Broad Spectrum SPF 1515 mL in 1 TUBESTICK154

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62839-620162839-6201-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

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
7003fce6-a062-4c13-8768-bfc4fa11f85100281d57-4b60-4485-bcb9-1aeca3e6630b2026-04-06WarningsExact identifier
spl id: 7003fce6-a062-4c13-8768-bfc4fa11f851
spl set id: 00281d57-4b60-4485-bcb9-1aeca3e6630b

Reported adverse events (FAERS/openFDA)#

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