FDA.reportPublic FDA data

GZE SKIN SMOOTHING SERUM

Manufacturer
Guangzhou Yilong Cosmetics Co., Ltd
Effective date
2024-10-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:53:17

Label at a glance#

ProductGZE SKIN SMOOTHING SERUM
Active ingredientBORNEOL, SALICYLIC ACID
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 1.5%

Borneol 1%

INACTIVE INGREDIENT SECTION

Coptis Extract

Phellodendron Chinense Extract

Acoruscalamus Extract

Honeysuckle Extract

Glycerol

Peppermint

OTC - PURPOSE SECTION

Keep your skin free of irritants, and keep the keratin in your skin from overproducing.

INDICATIONS & USAGE SECTION

Apply our skin smoothing serum daily after cleansing and toning. Twice a day for at least 4 weeks. Dispense apea-size amount of thees sence onto the problematic areas and use fingertips to massage slightly until completely absorbed.

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

Apply our skin smoothing serum daily after cleansing and toning. Twice a day for at least 4 weeks. Dispense apea-size amount of thees sence onto the problematic areas and use fingertips to massage slightly until completely absorbed.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product imageproduct image

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74458-117GZE SKIN SMOOTHING SERUM (SALICYLIC ACID 1.5% BORNEOL 1%) LIQUID [GUANGZHOU YILONG COSMETICS CO., LTD]1Unmatched20241008_23b7190c-c89c-5ef3-e063-6294a90a040e.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74458-11774458-117-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
COPTIS DELTOIDEA ROOT1UIP402HTIIACT
ACORUS CALAMUS WHOLEQ46A6NDR5CIACT
BORNEOLM89NIB437XACTIB
PEPPERMINTV95R5KMY2BIACT
SALICYLIC ACIDO414PZ4LPZACTIB
LONICERA CONFUSA FLOWER3JV904IJ0VIACT
PHELLODENDRON CHINENSE WHOLEQKA3ZK8IIEIACT
GLYCERINPDC6A3C0OXIACT

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
3b390827-00b4-6e6c-e063-6294a90a274923b7190c-c89c-5ef3-e063-6294a90a040e2025-07-31WarningsExact identifier
spl set id: 23b7190c-c89c-5ef3-e063-6294a90a040e

Reported adverse events (FAERS/openFDA)#

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