FDA.reportPublic FDA data

GZE AFTER SUN BODY BUTTER

Manufacturer
Guangzhou Yilong Cosmetics Co.,Ltd.
Effective date
2024-06-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:01:10

Label at a glance#

ProductGZE AFTER SUN BODY BUTTER
Active ingredientMATRICARIA CHAMOMILLA, BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES

MATRICARIA CHAMOMILLA

OTC - PURPOSE SECTION

Ultra rich moisturizers leave your skin hydrated for 12 hours.

INDICATIONS & USAGE SECTION

Apply a suffcient amount of butter onto cleansed face, neck and body. Gently massage into skin until fully absorbed. Use daily.

WARNINGS SECTION

For external use only.

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

Apply a suffcient amount of butter onto cleansed face, neck and body. Gently massage into skin until fully absorbed. Use daily.

INACTIVE INGREDIENT SECTION

COCO-CAPRYLATEICAPRATE
DIMETHICONE
PEG-9 DIGLYCIDYL ETHERISODIUM HYALURONATE CROSSPOLYMER
GLYCERIN
POTASSIUM SORBATE
CETYLALCOHOL
CETYL ESTERS WAX
WATER

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83566-210GZE AFTER SUN BODY BUTTER (BUTYROSPERMUM PARKII (SHEA) BUTTER) CREAM [GUANGZHOU YILONG COSMETICS CO.,LTD.]2Unmatched20240606_19f95bbf-fad8-609e-e063-6394a90a2cd3.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
83566-21083566-210-01

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
COCO-CAPRYLATE/CAPRATE8D9H4QU99HIACT
MATRICARIA CHAMOMILLAG0R4UBI2ZZACTIB
BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES0C9AC7D6XUACTIB
DIMETHICONE92RU3N3Y1OIACT
PEG-9 DIGLYCIDYL ETHER/SODIUM HYALURONATE CROSSPOLYMER788QAG3W8AIACT
GLYCERINPDC6A3C0OXIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
CETYL ALCOHOL936JST6JCNIACT
CETYL ESTERS WAXD072FFP9GUIACT
WATER059QF0KO0RIACT

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
39f3d484-1cff-abce-e063-6394a90a82f319f95bbf-fad8-609e-e063-6394a90a2cd32025-07-15WarningsExact identifier
spl set id: 19f95bbf-fad8-609e-e063-6394a90a2cd3

Reported adverse events (FAERS/openFDA)#

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