FDA.reportPublic FDA data

STYE RELIEF SERUM

Manufacturer
Guangzhou Shimei Cosmetics Co., Ltd.
Effective date
2025-12-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:25:42

Label at a glance#

ProductSTYE RELIEF SERUM
Active ingredientCARBOXYMETHYLCELLULOSE SODIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients CarboxymethylcelluloseSodium(CMC) 0.5% Purpose Emollient

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

OTC - PURPOSE SECTION

Helps with styes

Soothes lrritation

Gentle Formula

WARNINGS SECTION

For external use only.

INDICATIONS & USAGE SECTION

temporarily relieves burningand irritation of the eye.prevent further irritation ofthe eye.

DOSAGE & ADMINISTRATION SECTION

Directions
Take an appropriate amountand apply it to the skin aroundthe eyelid.

INACTIVE INGREDIENT SECTION

Inactive ingredients
Aqua(Water),Gentiana ScabraRoot Extract,Mentha Piperita(Peppermint)LeafWater,PipeMethysticum Leaf/Root/StemExtract,Sodium Hyaluronate,Taurine,ChamomillaRecutita(Matricaria) FlowerExtract,Viola Yedoensis Extract,Paeonia Albiflora Root Extract,Lonicera Japonica (Honeysuckle)Flower Extract,Taraxacum Officinale(Dandelion)Rhizome/Root Extract,Malva Sylvestris(Mallow)Flower Extract,AloeBarbadensis Leaf Juice,
Chondrus Crispus Extract,
Sodium Acetylated
Hyaluronate,HydrolyzedHyaluronic Acid,HyaluronicAcid,Sodium HyaluronateCrosspolymer,HydrolyzedSodium Hyaluronate,Potassium Hyaluronate.PVP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87183-001-01STYE RELIEF SERUM30 mL in 1 BOTTLEPASTE301

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87183-00187183-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
TARAXACUM OFFICINALE (DANDELION) ROOT9DE5YCO0RUIACT
HYALURONIC ACIDS270N0TRQYIACT
GENTIANA SCABRA ROOTGXZ33VNT92IACT
CARBOXYMETHYLCELLULOSE SODIUMK679OBS311ACTIB
HUMAN SKIN PROTEINS, PARTIALLY HYDROLYZEDG9813R29TWIACT
CHONDRUS CRISPUS CARRAGEENANUE856F2T78IACT
POTASSIUM HYPOPHOSPHITEB2Q648IJ6SIACT
AQUA059QF0KO0RIACT
MATRICARIA CHAMOMILLA WHOLEG0R4UBI2ZZIACT
LONICERA JAPONICA FLOWER4465L2WS4YIACT
VIOLA PHILIPPICA WHOLEO176VC3N54IACT
SODIUM ACETYLATED HYALURONATEWN66R7GL93IACT
PVPFZ989GH94EIACT
PIPER METHYSTICUM ROOTBOW48C81XPIACT
PAEONIA LACTIFLORA ROOT3Z3866YW6PIACT
MALVA SYLVESTRIS FLOWERING TOPX1U1U0N90JIACT
MENTHA PIPERITA (PEPPERMINT) LEAFA389O33LX6IACT
SODIUM HYALURONATEYSE9PPT4THIACT
TAURINE1EQV5MLY3DIACT
ALOE BARBADENSIS LEAF POWDERZY81Z83H0XIACT

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
STYE RELIEF SERUMCARBOXYMETHYLCELLULOSE SODIUM(CMC)Guangzhou Shimei Cosmetics Co., Ltd.45fa7962-b489-4613-e063-6394a90a59b02025-12-15WarningsExact identifier
ndc (package): 87183-001-01
ndc (product): 87183-001
ndc11 (package): 87183000101
spl id: 45fa7962-b48a-4613-e063-6394a90a59b0
spl set id: 45fa7962-b489-4613-e063-6394a90a59b0

Reported adverse events (FAERS/openFDA)#

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