FDA.reportPublic FDA data

GZE Multi-Effect Whitening Sunscreen

Manufacturer
Guangzhou Yilong Cosmetics Co.,Ltd.
Effective date
2024-06-07
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:00:56

Label at a glance#

ProductGZE Multi-Effect Whitening Sunscreen
Active ingredientASCORBIC ACID, TITANIUM DIOXIDE, ZINC OXIDE, CANNABIS SATIVA LEAF
Label structure11 sections

Indications and uses

Apply liberally 15 minutes before sun exposure.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Cannabis Sativa Leaf Extract 15.36%

Ascorbic Acid 10%

Titanium Dioxide 10%

Zinc Oxide 10%

Niacinamide 2%

Purpose

OTC - PURPOSE SECTION

For sunscreen use.

Uses

INDICATIONS & USAGE SECTION

Apply liberally 15 minutes before sun exposure.

WARNINGS

WARNINGS SECTION

For external use only.

Stop use and ask a doctor if

OTC - STOP USE SECTION

rash occurs.

Do not use

OTC - DO NOT USE SECTION

Do not use on damaged or broken.

When using this product

OTC - WHEN USING SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Squeeze out an appropriate amount of sunscreen and spread evenly on skin.

INACTIVE INGREDIENT SECTION

NIACINAMIDE
GLYCERIN
WATER O-15
PEG-9 DIGLYCIDYL ETHERISODIUM HYALURONATE CROSSPOLYMER
TREHALOSE
ALLANTOIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-122GZE MULTI-EFFECT WHITENING SUNSCREEN (TITANIUM DIOXIDE,ZINC OXIDE) CREAM [GUANGZHOU YILONG COSMETICS CO.,LTD.]4Unmatched20240609_16c031d5-cdef-3350-e063-6294a90aea7c.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-12283566-122-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
NIACINAMIDE25X51I8RD4IACT
ASCORBIC ACIDPQ6CK8PD0RACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
GLYCERINPDC6A3C0OXIACT
ZINC OXIDESOI2LOH54ZACTIB
WATER O-1563M8RYN44NIACT
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER788QAG3W8AIACT
TREHALOSEB8WCK70T7IIACT
ALLANTOIN344S277G0ZIACT
CANNABIS SATIVA LEAFA718Z7DA1KACTIB

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
39f09235-94b0-244b-e063-6294a90a05f616c031d5-cdef-3350-e063-6294a90aea7c2025-07-14WarningsExact identifier
spl set id: 16c031d5-cdef-3350-e063-6294a90aea7c

Reported adverse events (FAERS/openFDA)#

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