SEE CLEAN-ONE EYE DROPS- boric acid liquid 
Cho-A Pharm.Co.,Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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See Clean-One Eye Drops

Active ingredient

Boric acid (1.546mg/1ml)

Purpose

Lubricant

Uses

For the temporarily relief of

- burning and irritation due to dryness of the eye

- redness of the eye due to minor eye irritation

Warnings

For external use only

Do not use

- if this product changes color or becomes cloudy

- if you are sensitive to any ingredient in this product

When using this product

- do not touch tip of container to any surface to avoid contamination

- remove contact lenses before using

- replace cap after use

Stop use and ask a doctor if

- you experience eye pain, changes in vision, continued redness or irritation of the eye

- conditions worsen

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

Instill 1-3 drops in the affected eye(s) 3-6 times a day

Inactive ingredients

Sulfamethoxazole, dipotassium glycyrrhizinate, Chlorpheniramine Maleate, Aminocaproic Acid, Disodium Edetate Hydrate, Sodium Tetraborate, Sodium hydroxide, Sterile Water for Injection

See Clean-One Eye Drops

see clean one eye drops

SEE CLEAN-ONE EYE DROPS 
boric acid liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58354-105
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BORIC ACID (UNII: R57ZHV85D4) (BORIC ACID - UNII:R57ZHV85D4) BORIC ACID21.644 mg  in 14 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BORATE ANHYDROUS (UNII: 8191EN8ZMD)  
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
WATER (UNII: 059QF0KO0R)  
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z)  
AMINOCAPROIC ACID (UNII: U6F3787206)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
SULFAMETHOXAZOLE (UNII: JE42381TNV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58354-105-021 in 1 BOX12/29/2017
1NDC:58354-105-0114 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other12/29/201705/18/2023
Labeler - Cho-A Pharm.Co.,Ltd. (688056831)
Registrant - Cho-A Pharm.Co.,Ltd. (688056831)
Establishment
NameAddressID/FEIBusiness Operations
Cho-A Pharm.Co.,Ltd.688056831manufacture(58354-105)

Revised: 5/2023
 
Cho-A Pharm.Co.,Ltd.