Label: MURO 128- sodium chloride solution
- NDC Code(s): 24208-277-15, 24208-277-30, 24208-277-59
- Packager: Bausch & Lomb Incorporated
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 Label Information
Updated May 25, 2022
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
For external use only
Do not use
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- except under the advice and supervision of a doctor
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- if solution changes color or becomes cloudy
When using this product
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- it may cause temporary burning and irritation
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- to avoid contamination, do not touch tip of container to any surface
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- replace cap after use
Stop use and ask a doctor if
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- condition worsens or persists for more than 72 hours
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- you experience eye pain, changes in vision, continued redness or irritation of the eye
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
- Package/Label Principal Display Panel – Muro 128 15 mL
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INGREDIENTS AND APPEARANCE
MURO 128
sodium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24208-277 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 50 mg in 1 mL Inactive Ingredients Ingredient Name Strength BORIC ACID (UNII: R57ZHV85D4) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BORATE (UNII: 91MBZ8H3QO) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24208-277-15 1 in 1 CARTON 01/01/2011 1 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:24208-277-30 1 in 1 CARTON 01/01/2011 01/01/2020 2 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:24208-277-59 1 in 1 CARTON 01/01/2011 3 2 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part349 01/01/2011 Labeler - Bausch & Lomb Incorporated (196603781) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Incorporated 079587625 MANUFACTURE(24208-277)