DriEyes LUBRICANT EYE DROPS by Jiangxi Hemei Pharmaceutical Co., Ltd 84010-095 complete

DriEyes LUBRICANT EYE DROPS by

Drug Labeling and Warnings

DriEyes LUBRICANT EYE DROPS by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DRIEYES LUBRICANT EYE DROPS- carboxymethylcellulose sodium 0.50% lubricant eye drops liquid 
Jiangxi Hemei Pharmaceutical Co., Ltd

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84010-095 complete

Active Ingredient

Carboxymethylcellulose sodium 0.50%

Purpose

Lubricant

Use

·For use as a protectant against further irritation or to relieve dryness ofthe eye.

·For the temporary relief of burning & irritation due to the dryness of the eye.

·Relieves redness of the eye due to minor eye irritations.

Warnings

For external use only.

Do not use

if solution changes color or becomes cloudy.

When Using

·To avoid contamination, do not touch tip of container to any surface.
·Replace cap after using.

Stop Use

·you experience eye pain
·you experience changes in vision
·you experience continued redness orirritation of the eye
·the condition worsens
·symptoms last for more than 72 hours

Ask Doctor

if you have narrow angle glaucoma

Keep Oot Of Reach Of Children

lf swallowed, get medical help or contact a Poison Control Center right away.

Directions

Instill 1 to 2 drops in the affected eye(s) up to four times daily.

Other information

· Store at room temperature.
· Remove contact lenses before using.

·Do not use if neckband on bottle is broken or missing

Inactive ingredients

Water、Sodium Hyaluronate、Boric acid、Borax、Borneol、Methylparaben、Ethanol

PRINCIPAL DISPLAY PANEL

1

DRIEYES LUBRICANT EYE DROPS 
carboxymethylcellulose sodium 0.50% lubricant eye drops liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 84010-095
Route of AdministrationINTRAOCULAR
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) (CARBOXYMETHYLCELLULOSE - UNII:05JZI7B19X) CARBOXYMETHYLCELLULOSE SODIUM0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BORIC ACID (UNII: R57ZHV85D4)  
ALCOHOL (UNII: 3K9958V90M)  
BORNEOL (UNII: M89NIB437X)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
SODIUM BORATE (UNII: 91MBZ8H3QO)  
SODIUM HYALURONATE (UNII: YSE9PPT4TH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 84010-095-0115 mL in 1 BOTTLE; Type 0: Not a Combination Product03/28/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01803/28/202502/08/2026
Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)
Establishment
NameAddressID/FEIBusiness Operations
Jiangxi Hemei Pharmaceutical Co., Ltd724892056manufacture(84010-095)

Revised: 2/2026