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Murocel

Dosage form: solution/ drops
Ingredients: METHYLCELLULOSE (4000 CPS) 10mg in 15mL
Labeler: Bausch & Lomb Incorporated
NDC Code: 24208-280

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.

Drug Facts

Active Ingredient

Methylcellulose 10 mg (1%)

Purpose

Lubricant

Uses

temporary relief of burning and irritation due to dryness of the eye

Warnings

Do not use

if solution changes color or becomes cloudy

When using this product
  • do not touch tip of container to any surface to avoid contamination
  • replace cap after use

Stop use and ask doctor if
  • you experience eye pain, changes in vision, continued redness or irritation of the eye
  • condition 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.

Directions

instill 1 to 2 drops in the affected eye(s) as needed

Other information
  • store at 15º – 30ºC (59º – 86ºF)
  • keep tightly closed

Inactive ingredients

boric acid, propylene glycol, sodium borate, sodium chloride, purified water, hydrochloric acid and/or sodium hydroxide may be added to adjust pH.

PRESERVATIVES ADDED: methylparaben 0.028%, propylparaben 0.012%.

Package/Label Principal Display Panel

NDC 24208-280-15

BAUSCH & LOMB

Murocel®

Methylcellulose
Lubricant
Ophthalmic Solution
USP, 1%

[icon- eye]

STERILE

FOR USE IN THE EYES ONLY

1/2 FL. OZ. (15 mL)

MUROCEL 
methylcellulose solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:24208-280
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
METHYLCELLULOSE (4000 CPS) (METHYLCELLULOSE (4000 CPS)) METHYLCELLULOSE (4000 CPS)10 mg  in 15 mL
Inactive Ingredients
Ingredient NameStrength
BORIC ACID 
PROPYLENE GLYCOL 
SODIUM BORATE 
SODIUM CHLORIDE 
WATER 
METHYLPARABEN 
PROPYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:24208-280-151 BOTTLE, DROPPER (BOTTLE) in 1 CARTON
115 mL in 1 BOTTLE, DROPPER
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34905/04/2011
Labeler - Bausch & Lomb Incorporated (196603781)
Establishment
NameAddressID/FEIOperations
Bausch & Lomb Incorporated807927397MANUFACTURE

Revised: 05/2011
Document Id: ee0bf442-2b50-4299-87fb-063d60df28e5
Set id: ee0bf442-2b50-4299-87fb-063d60df28e5
Version: 1
Effective Time: 20110504
 
Bausch & Lomb Incorporated

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 drug combination in no way should be construed to indicate that the drug or drug combination is safe, effective or appropriate for any given patient. If you have questions about the drugs you are taking, check with your doctor, nurse or pharmacist.

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