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
Drug Label Information
Updated September 25, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only
Do not use
- except under the advice and supervision of a doctor
- if solution changes color or becomes cloudy
When using this product
- it may cause temporary burning and irritation
- to avoid contamination, do not touch tip of container to any surface
- replace cap after use
Stop use and ask a doctor if
- condition worsens or persists for more than 72 hours
- 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
-
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 Drug M018 01/01/2011 Labeler - Bausch & Lomb Incorporated (196603781) Establishment Name Address ID/FEI Business Operations Bausch & Lomb Incorporated 079587625 manufacture(24208-277)