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lubricating plus by Major Pharmaceuticals

Medically reviewed on July 12, 2016

Dosage form: solution/ drops
Ingredients: CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM 0.5g in 100mL
Labeler: Major Pharmaceuticals
NDC Code: 0904-6329

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Major Pharmaceuticals Lubricating Plus Drug Facts

Active ingredient (in each single-use container)

Carboxymethylcellulose sodium 0.5%

Purpose

Eye lubricant

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

Warnings

For external use only

Do not use

if solution changes color or becomes cloudy

When using this product

to avoid contamination

do not touch tip of container to any surface
do not reuse
once opened, discard
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 reach of children.

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

Directions
to open, twist and pull tab to remove
instill 1 or 2 drops in the affected eye(s) as needed and discard container

Other information
store at 20-25°C (68-77°F)
RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive Ingredients

calcium chloride dihydrate, magnesium chloride hexahydrate, potassium chloride, sodium chloride, sodium lactate solution, water for injection. May also contain sodium hydroxide and/or hydrochloric acid to adjust pH.

Questions or comments?

1-800-616-2471

Package/Label Principal Display Panel

COMPARE TO the active ingredient of REFRESH PLUS®

preservative-Free

Lubricating PLUS

Lubricant Eye Drops

Immediate, soothing relief for dry eyes

Moisturizing Relief

Carboxymethylcellulose Sodium 0.5%

30 Sterile Single-Use Containers

0.01 FL OZ (0.4 mL) each

Actual Size

LUBRICATING PLUS 
carboxymethylcellulose sodium solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0904-6329
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (CARBOXYMETHYLCELLULOSE) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM0.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CALCIUM CHLORIDE 
MAGNESIUM CHLORIDE 
POTASSIUM CHLORIDE 
SODIUM CHLORIDE 
SODIUM LACTATE 
WATER 
SODIUM HYDROXIDE 
HYDROCHLORIC ACID 
Packaging
#Item CodePackage Description
1NDC:0904-6329-466 POUCH in 1 CARTON
15 VIAL, SINGLE-USE in 1 POUCH
10.4 mL in 1 VIAL, SINGLE-USE
2NDC:0904-6329-5110 POUCH in 1 CARTON
25 VIAL, SINGLE-USE in 1 POUCH
20.4 mL in 1 VIAL, SINGLE-USE
3NDC:0904-6329-5814 POUCH in 1 CARTON
35 VIAL, SINGLE-USE in 1 POUCH
30.4 mL in 1 VIAL, SINGLE-USE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34905/09/2013
Labeler - Major Pharmaceuticals (191427277)

 
Major Pharmaceuticals

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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