FDA.reportPublic FDA data

Centella Sunscreen SPF 50

Manufacturer
Guangzhou Yueyou Biological Technology Co., Ltd.
Effective date
2025-07-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:07:15

Label at a glance#

ProductCentella Sunscreen SPF 50
Active ingredientDROMETRIZOLE TRISILOXANE, METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE, ETHYLHEXYL TRIAZONE
Label structure7 sections

Label contents#

Full prescribing information#

Centella Sunscreen SPF 50

DOSAGE & ADMINISTRATION SECTION

Apply generously as the laststep in your skincare routine.Reapply every 2 hours when
exposed to sunlight. dosagedosage

WARNING

WARNINGS SECTION

For external use only. Avoid direct contact with eyes. Discontinue use if irritation occurs.

warningwarning

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT

inactive ingredientsinactive ingredients

Usage

INDICATIONS & USAGE SECTION

how to use

Apply generously as the laststep in your skincare routineReapply every 2 hours whenexposed to sunlight.

usageusage

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN keep reach out of childrenkeep reach out of children

Purpose

OTC - PURPOSE SECTION

purposepurpose

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Centella Sunscreen SPF 50Centella Sunscreen SPF 50

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85473-442-50Centella Sunscreen SPF 5050 g in 1 TUBECREAM501

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
85473-44285473-442-50

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
SODIUM HYALURONATEYSE9PPT4THIACT
DROMETRIZOLE TRISILOXANEHC22845I1XACTIB
MADECASSOSIDECQ2F5O6YIYIACT
METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL8NT850T0YSACTIB
LICORICE61ZBX54883IACT
GREEN TEA LEAFW2ZU1RY8B0IACT
BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINEPWZ1720CBHACTIB
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATEANQ870JD20ACTIB
TREMELLA FUCIFORMIS FRUITING BODYGG8N28393GIACT
WATER059QF0KO0RIACT
TOCOPHEROLR0ZB2556P8IACT
CENTELLA ASIATICA LEAF6810070TYDIACT
HOUTTUYNIA CORDATA FLOWERING TOPRH041UUZ22IACT
GLYCERINPDC6A3C0OXIACT
NIACINAMIDE25X51I8RD4IACT
PANTHENOLWV9CM0O67ZIACT
ALLANTOIN344S277G0ZIACT
PORTULACA OLERACEA LEAF9JW9D9JGHZIACT
ETHYLHEXYL TRIAZONEXQN8R9SAK4ACTIB
HYALURONIC ACIDS270N0TRQYIACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT

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
39f28d7d-7b23-16b5-e063-6394a90abc1639f28d7d-7b22-16b5-e063-6394a90abc162025-07-15WarningsExact identifier
spl id: 39f28d7d-7b23-16b5-e063-6394a90abc16
spl set id: 39f28d7d-7b22-16b5-e063-6394a90abc16

Reported adverse events (FAERS/openFDA)#

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