FDA.reportPublic FDA data

Sun Serum Drops

Manufacturer
Better Planet Brands LLC
Effective date
2026-10-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
daily-update
Hydrated at
2026-10-17 02:02:23

Label at a glance#

ProductSun Serum Drops
Active ingredientZINC OXIDE
Label structure7 sections

Indications and uses

• helps prevent sunburn

Label contents#

Full prescribing information#

Purpose

OTC - PURPOSE SECTION

Sunscreen

Uses

INDICATIONS & USAGE SECTION

• helps prevent sunburn

Warnings

WARNINGS SECTION

• For external use

OTC - DO NOT USE SECTION

• Do not use on damaged or broken skin.

OTC - DO NOT USE SECTION

OTC - STOP USE SECTION

• 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.

Other information

OTHER SAFETY INFORMATION

• Protect this product from excessive heat and direct sun. • May stain some

Inactive Ingredients

INACTIVE INGREDIENT SECTION

DICAPRYLYL CARBONATE, CAPRYLIC/CAPRIC TRIGLYCERIDE, BUTYLOCTYL SALICYCLATE, TRIDECTYL SALICYCLATE, COCO-CAPRYLATE/ CAPRATE, COCONUT ALKANES, SORBITAN SESQUIOLEATE, POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE, BUTYROSPERMUM PARKII (SHEA) BUTTER*, CETYL ALCOHOL, STEARYL ALCOHOL,

TOCOPHERYL ACETATE (VITAMIN E), CALENDULA OFFICINALIS (POT MARIGOLD) FLOWER, OLEA EUROPEA (OLIVE) FRUIT OIL, LECITHIN, ETHYLHEXYGLYCERIN.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 877.902.2873

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54136-37154136-371-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
ZINC OXIDESOI2LOH54ZACTIB
COCONUT ALKANES1E5KJY107TIACT
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
STEARYL ALCOHOL2KR89I4H1YIACT
TRIDECYL SALICYLATEAZQ08K38Z1IACT
BUTYROSPERMUM PARKII (SHEA) BUTTERK49155WL9YIACT
CALENDULA OFFICINALIS FLOWERP0M7O4Y7YDIACT
SOYBEAN LECITHIN1DI56QDM62IACT
OLEA EUROPAEA (OLIVE) FRUIT OIL6UYK2W1W1EIACT
CETYL ALCOHOL936JST6JCNIACT
BUTYLOCTYL SALICYLATE2EH13UN8D3IACT
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE9229XJ4V12IACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
DICAPRYLYL CARBONATE609A3V1SUAIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
CAPRYLIC/CAPRIC TRIGLYCERIDEC9H2L21V7UIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-12-03full-release2026-06-01 01:19:16

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
451328b0-2ca7-b0f4-e063-6294a90a03dd2cdb97bf-a4d7-1cb7-e063-6394a90ab2b82025-12-03WarningsExact identifier
spl set id: 2cdb97bf-a4d7-1cb7-e063-6394a90ab2b8

Reported adverse events (FAERS/openFDA)#

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