STYE RELIEF SERUM (carboxymethylcellulose sodium- cmc paste

STYE RELIEF SERUM by

Drug Labeling and Warnings

STYE RELIEF SERUM by is a Otc medication manufactured, distributed, or labeled by Guangzhou Shimei Cosmetics Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients CarboxymethylcelluloseSodium(CMC) 0.5% Purpose Emollient

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

PURPOSE

Helps with styes

Soothes lrritation

Gentle Formula

WARNINGS

For external use only.

INDICATIONS & USAGE

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

DOSAGE & ADMINISTRATION

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

INACTIVE INGREDIENT

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

STYE RELIEF SERUM 
carboxymethylcellulose sodium(cmc) paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87183-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X)	CARBOXYMETHYLCELLULOSE SODIUM	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
TARAXACUM OFFICINALE (DANDELION) ROOT (UNII: 9DE5YCO0RU)
HYALURONIC ACID (UNII: S270N0TRQY)
GENTIANA SCABRA ROOT (UNII: GXZ33VNT92)
HUMAN SKIN PROTEINS, PARTIALLY HYDROLYZED (UNII: G9813R29TW)
CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
POTASSIUM HYPOPHOSPHITE (UNII: B2Q648IJ6S)
AQUA (UNII: 059QF0KO0R)
MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)
LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
VIOLA PHILIPPICA WHOLE (UNII: O176VC3N54)
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)
PVP (UNII: FZ989GH94E)
PIPER METHYSTICUM ROOT (UNII: BOW48C81XP)
PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)
MALVA SYLVESTRIS FLOWERING TOP (UNII: X1U1U0N90J)
MENTHA PIPERITA (PEPPERMINT) LEAF (UNII: A389O33LX6)
SODIUM HYALURONATE (UNII: YSE9PPT4TH)
TAURINE (UNII: 1EQV5MLY3D)
ALOE BARBADENSIS LEAF POWDER (UNII: ZY81Z83H0X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87183-001-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M018	12/15/2025

Labeler - Guangzhou Shimei Cosmetics Co., Ltd. (530141589)

Registrant - Guangzhou Shimei Cosmetics Co., Ltd. (530141589)