FDA.reportPublic FDA data

Sun Bum Coconut Lip 30 Tinted Sunscreen Lip Balm - Bonfire

Manufacturer
Sun Bum, LLC
Effective date
2026-06-25
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-07-17 21:36:05

Label at a glance#

ProductSun Bum Coconut Lip 30 Tinted Sunscreen Lip Balm - Bonfire
Active ingredientAVOBENZONE, OCTISALATE, OCTOCRYLENE, HOMOSALATE
Label structure15 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 • children under 6 months of age: ask a doctor • 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 value of 15 or higher and...

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

AVOBENZONE 3%, HOMOSALATE 10%, OCTISALATE 5%, OCTOCRYLENE 8%

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

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

Stop use and ask a doctor if rash occurs

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Warnings

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of Reach Of Children

Directions

INSTRUCTIONS FOR USE 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

• children under 6 months of age: ask a doctor

• 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 value 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

Directions

DOSAGE & ADMINISTRATION SECTION

• apply liberally 15 minutes before sun exposure

Other Information

OTHER SAFETY INFORMATION

protect this product from excessive heat and direct sun

Inactive Ingredients

INACTIVE INGREDIENT SECTION

CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER, CANOLA OIL, SILICA, RICINUS COMMUNIS (CASTOR) SEED OIL, POLYHYDROXYSTEARIC ACID, ALOE BARBADENSIS LEAF EXTRACT, ARGANIA SPINOSA KERNEL OIL, BISABOLOL, BORON NITRIDE, EUPHORBIA CERIFERA (CANDELILLA) WAX, FRAGRANCE, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, HELIANTHUS ANNUUS (SUNFLOWER) SEED WAX, SACCHARIN, TOCOPHEROL ACETATE, ZINC OXIDE, MAY CONTAIN: IRON OXIDES, RED 6, RED 7, RED 28 LAKE

Questions?

OTC - QUESTIONS SECTION

1-877-978-6286

Sun Bum Coconut Lip 30 Tinted Sunscreen Lip Balm - Bonfire Primary Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Primary ArtworkPrimary Artwork

Sun Bum Coconut Lip 30 Tinted Sunscreen Lip Balm - Cocoa Beach Primary Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Primary ArtworkPrimary Artwork

Sun Bum Coconut Lip 30 Tinted Sunscreen Lip Balm - Heat Wave Primary Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Primary ArtworkPrimary Artwork

Sun Bum Coconut Lip 30 Tinted Sunscreen Lip Balm - Sunset Cove Primary Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Primary ArtworkPrimary Artwork

Sun Bum Coconut Lip 30 Tinted Sunscreen Lip Balm - Sunset Cove 2 Pack Primary Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Primary ArtworkPrimary Artwork

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69039-83069039-830-01, 69039-830-02
69039-83169039-831-01, 69039-831-02
69039-83369039-833-01, 69039-833-02
69039-83269039-832-01, 69039-832-02
69039-84269039-842-01, 69039-842-02

Ingredients#

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

DailyMed ingredient rows page 1 of 3 · 115 matching rows.

Name, UNII, Kind table
NameUNIIKind
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)N7YC58165TIACT
ARGANIA SPINOSA KERNEL OIL4V59G5UW9XIACT
EUPHORBIA CERIFERA (CANDELILLA) WAXWL0328HX19IACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
ZINC OXIDESOI2LOH54ZIACT
FERRIC OXIDE RED1K09F3G675IACT
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
CANOLA OIL331KBJ17RKIACT
RICINUS COMMUNIS (CASTOR) SEED OILD5340Y2I9GIACT
RED 7ECW0LZ41X8IACT
HELIANTHUS ANNUUS SEED WAX42DG15CHXVIACT
SACCHARINFST467XS7DIACT
ALOE BARBADENSIS LEAFZY81Z83H0XIACT
BISABOLOL24WE03BX2TIACT
BORON NITRIDE2U4T60A6YDIACT
RED 28767IP0Y5NHIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
HOMOSALATEV06SV4M95SACTIB
SILICAETJ7Z6XBU4IACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
RED 6481744AI4OIACT
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL3W1JG795YIIACT
RED 6481744AI4OIACT
CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S)N7YC58165TIACT
ARGANIA SPINOSA KERNEL OIL4V59G5UW9XIACT
EUPHORBIA CERIFERA (CANDELILLA) WAXWL0328HX19IACT
POLYHYDROXYSTEARIC ACID (2300 MW)YXH47AOU0FIACT
ZINC OXIDESOI2LOH54ZIACT
FERRIC OXIDE RED1K09F3G675IACT
AVOBENZONEG63QQF2NOXACTIB
OCTISALATE4X49Y0596WACTIB
OCTOCRYLENE5A68WGF6WMACTIB
CANOLA OIL331KBJ17RKIACT
RICINUS COMMUNIS (CASTOR) SEED OILD5340Y2I9GIACT
RED 7ECW0LZ41X8IACT
HELIANTHUS ANNUUS SEED WAX42DG15CHXVIACT
SACCHARINFST467XS7DIACT
ALOE BARBADENSIS LEAFZY81Z83H0XIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-08-28full-release2026-06-01 01:12:06

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
551b8b16-d7e1-c5d2-e063-6294a90a59fc3d4aeea5-62e2-6772-e063-6394a90adac82026-06-25WarningsExact identifier
spl id: 551b8b16-d7e1-c5d2-e063-6294a90a59fc
spl set id: 3d4aeea5-62e2-6772-e063-6394a90adac8

Reported adverse events (FAERS/openFDA)#

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