FDA.reportPublic FDA data

Gze MATRIXYL 3000 SERUM

Manufacturer
Guangzhou Yilong Cosmetics Co.,Ltd.
Effective date
2024-06-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:01:01

Label at a glance#

ProductGze MATRIXYL 3000 SERUM
Active ingredientPALMITOYL TETRAPEPTIDE-7, ACETYL HEXAPEPTIDE-8, PALMITOYL TRIPEPTIDE-1
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

PALMITOYL TETRAPEPTIDE-7 8%

PALMITOYL TRIPEPTIDE-1 8.7%

ACETYL HEXAPEPTIDE-8 5%

INACTIVE INGREDIENT SECTION

ALLANTOIN

NIACINAMIDE

ADENOSINE

GLYCERIN

PEG-9 DIGLYCIDYL ETHERISODIUM HYALURONATE CROSSPOLYMER

1.2-HEXANEDIOL
PROPANEDIOL
1.3-BETA-GLUCAN SYNTHASE COMPONENT FKS1
BUTYLENE GLYCOL
ROSA DAMASCENA FLOWER
ALOE ANDONGENSIS LEAF
LAVENDER OIL
CAMELLIA SINENSIS WHOLE

OTC - PURPOSE SECTION

Moisturizing.

INDICATIONS & USAGE SECTION

Wash and pat skin dry. Apply serum as needed.Use a small amount to massage into face and neck in circular motions. Allow to absorb. Suitable for daily use (morning and night).

WARNINGS SECTION

For external use only.

OTC - STOP USE SECTION

Stop use and ask a doctor if rash occurs.

OTC - DO NOT USE SECTION

Do not use on damaged or broken skin.

OTC - WHEN USING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

Suitable for daily use,twice a day (in the morning and night).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-087GZE MATRIXYL 3000 SERUM (PALMITOYL TRIPEPTIDE-1) LIQUID [GUANGZHOU YILONG COSMETICS CO.,LTD.]2Unmatched20240609_18f4abd0-b0c8-6fd1-e063-6294a90a1807.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83566-08783566-087-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZIACT
NIACINAMIDE25X51I8RD4IACT
ADENOSINEK72T3FS567IACT
GLYCERINPDC6A3C0OXIACT
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER788QAG3W8AIACT
PALMITOYL TETRAPEPTIDE-7Q41S464P1RACTIB
ACETYL HEXAPEPTIDE-8L4EL31FWILACTIB
1,2-HEXANEDIOLTR046Y3K1GIACT
PROPANEDIOL5965N8W85TIACT
1,3-BETA-GLUCAN SYNTHASE COMPONENT FKS14FRY3LJG0VIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ROSA DAMASCENA FLOWERJWB78P295AIACT
PALMITOYL TRIPEPTIDE-1RV743D216MACTIB
ALOE ANDONGENSIS LEAFN1P4NU25EJIACT
LAVENDER OILZBP1YXW0H8IACT
CAMELLIA SINENSIS WHOLEC5M4585ZBZIACT

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
39f27fa3-e6c0-0cfd-e063-6394a90a1c3818f4abd0-b0c8-6fd1-e063-6294a90a18072025-07-15WarningsExact identifier
spl set id: 18f4abd0-b0c8-6fd1-e063-6294a90a1807

Reported adverse events (FAERS/openFDA)#

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