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Medics Choice Lubricant Eye Drops

Medically reviewed by Drugs.com. Last updated on Jan 31, 2022.

Dosage form: solution
Ingredients: CARBOXYMETHYLCELLULOSE SODIUM 0.5g in 100mL
Labeler: K.C. Pharmaceuticals, Inc.
NDC Code: 55651-030

Medic's Ch. Lub Eye 5 Ct. Sgl Use

Active ingredients

carboxymethylcellulose sodium 0.5%

Purpose

Carboxymethylcellulose sodium......Lubricant

Uses

  • for the temporary relief of burning, irritation, and discomfort due to dryness of the eyes or exposure to wind or sun
  • may be used as a protectant against further irritation

Warnings

For external use only

Do not use this product if

  • solution changes color or becomes cloudy

When using this product

  • do not reuse
  • once opened, discard
  • to avoid contamination, do not touch tip of container to any surface
  • do not touch unit-dose tip to eye

Stop use and ask a doctor if

  • you experience eye pain
  • changes in vision occur
  • redness or irritation of the eye continues
  • redness or irritation of the eye worsens or persists for more than 72 hours

Keep out of the reach of children. If accidentally swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately.

Directions

  • to open, twist and pull tab to remove
  • instill 1 or 2 drops in the affected eye(s) as needed and discard container
  • if used for post-operative (e.g., LASIK) dryness and discomfort, follow yur eye doctor's instructions

Other information

  • store at 15º-25ºC (59º-77ºF)
  • use only if single-use container is intact
  • use before expiration date marked on container
  • RETAIN THIS CARTON FOR FUTURE REFERENCE

Inactive ingredients

calcium chloride, **hydrochloric acid, magnesium chloride, potassium chloride, purified water, sodium chloride, **sodium hydroxide, sodium lactate.

**may contain these ingredients to adjust pH.

MEDICS CHOICE LUBRICANT EYE DROPS 
carboxymethylcellulose sodium solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55651-030
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM (CARBOXYMETHYLCELLULOSE) CARBOXYMETHYLCELLULOSE SODIUM0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM LACTATE 
SODIUM CHLORIDE 
HYDROCHLORIC ACID 
MAGNESIUM CHLORIDE 
WATER 
SODIUM HYDROXIDE 
CALCIUM CHLORIDE 
POTASSIUM CHLORIDE 
Packaging
#Item CodePackage Description
1NDC:55651-030-015 AMPULE in 1 CARTON
10.4 mL in 1 AMPULE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34902/10/2020
Labeler - K.C. Pharmaceuticals, Inc. (174450460)
Establishment
NameAddressID/FEIOperations
K.C. Pharmaceuticals, Inc.174450460manufacture(55651-030), pack(55651-030), label(55651-030)

Document Id: 9df453eb-7359-9219-e053-2995a90a23bb
Set id: 9ddfc275-602f-413b-e053-2995a90a11cb
Version: 2
Effective Time: 20200210
 
K.C. Pharmaceuticals, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer