Otc - Active Ingredient
Active ingredients CarboxymethylcelluloseSodium(CMC) 0.5% Purpose Emollient
Stye Relief Serum Paste
FDA Label NDC 87183-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Shimei Cosmetics Co., Ltd. for the product Stye Relief Serum (NDC 87183-001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - keep out of reach of children, otc - purpose, warnings, indications & usage, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
Otc - 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
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