FDA.reportPublic FDA data

Sun Bum Sunscreen Lip Balm Broad Spectrum SPF 30

Manufacturer
Sun Bum LLC
Effective date
2019-10-16
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 00:07:13

Label at a glance#

ProductSun Bum Sunscreen Lip Balm Broad Spectrum SPF 30 Coconut
Active ingredientAVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE
Label structure9 sections

Indications and uses

Helps prevent sunburn. 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 exposure Reapply: After 80 minutes of swimming or sweating. Immediately after towel drying. At least every 2 hours Sun Protection 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. Sun Proection Measures including...

Storage and handling

Protect this product from excessive heat and direct sun.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Avobenzone 2.00%

Homosalate 15.00%

Octinoxate 7.50%

Octissalate 5.00%

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • Helps prevent sunburn.
  • 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.
  • Do not use on damaged or broken skin.
  • Stop use and ask a doctor if rash occurs.

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 exposure
  • Reapply:
  • After 80 minutes of swimming or sweating.
  • Immediately after towel drying.
  • At least every 2 hours

Sun Protection 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.

Sun Proection Measures

including:

  • Limit time in the sun, especially from 10 am - 2 pm.
  • Wear long-sleeve shirts, pants, hats, and sunglasses.
  • Children under 6 months: Ask a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Adipic Acid / Diglycol Crosspolymer, Aloe Barbadensis Leaf Extract, Ascorbic Acid, BHT, Calendula Officinalis Flower Extract, Cameilia Sinensis Leaf Extract, Caprylic / Capric Triglyceride, Cetyl Alcohol, Citrus Grandis (Grapefruit) Fruit Extract, Citrus Limon (Lemon) Peel Extract, Cucumis Sativus (Cucumber) Fruit Extract, Cyclohexasiloxane, Cyclopentasiloxane, Diisobutyl Adipate, Dimethicone, Equisetum Extract, Hydrated Silica, Isostearyl Linoleate, Macrocystis Pyrifera (kelp) Extract, mineral Oil, Oxokarite, Panax Ginseng Root Extract, PEG-8, Polysorbate 80, Propylene Glycol, Punica Granatum (Pomegranate) Extract, Rosmarinus Officinalis (Rosemary) Extract, Saccharin, Salix Alba (Willow) Bark Extract, Salvia Officnialis (Sage) Extract, Thoabroma Cacao (Cocoa) Seed Butter, Tocopheryl Acetate, Water.

Other information

STORAGE AND HANDLING SECTION

  • Protect this product from excessive heat and direct sun.

Questions or Comments?

OTC - QUESTIONS SECTION

Call + 1 (877) 978-6286

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label1Label1Label2Label2

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69039-20469039-204-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
ADIPIC ACID76A0JE0FKJIACT
ALOE VERA LEAFZY81Z83H0XIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
GREEN TEA LEAFW2ZU1RY8B0IACT
CETYL ALCOHOL936JST6JCNIACT
GRAPEFRUITO82C39RR8CIACT
LEMON PEEL72O054U628IACT
CYCLOMETHICONE 6XHK3U310BAIACT
CYCLOMETHICONE 50THT5PCI0RIACT
DIMETHICONE92RU3N3Y1OIACT
EQUISETUM ARVENSE BRANCH1L0VKZ185EIACT
GINKGO19FUJ2C58TIACT
HYDRATED SILICAY6O7T4G8P9IACT
ISOSTEARYL LINOLEATE4778M3HR0NIACT
MACROCYSTIS PYRIFERAK31S3OG5C4IACT
MINERAL OILT5L8T28FGPIACT
CERESINQ1LS2UJO3AIACT
ASIAN GINSENGCUQ3A77YXIIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT
POLYSORBATE 806OZP39ZG8HIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
POMEGRANATE56687D1Z4DIACT
SACCHARINFST467XS7DIACT
WILLOW BARKS883J9JDYXIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
WATER059QF0KO0RIACT
AVOBENZONEG63QQF2NOXACTIB
HOMOSALATEV06SV4M95SACTIB
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB

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
d740403c-146e-dac9-e053-2995a90a1aec347a8d75-d6c9-4e9d-9649-982137d2d1592022-02-05WarningsExact identifier
spl set id: 347a8d75-d6c9-4e9d-9649-982137d2d159

Reported adverse events (FAERS/openFDA)#

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