- 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
-
INGREDIENTS AND APPEARANCE
MURO 128
sodium chloride solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24208-276 Route of Administration OPHTHALMIC Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CHLORIDE 20 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) HYDROCHLORIC ACID (UNII: QTT17582CB) SODIUM HYDROXIDE (UNII: 55X04QC32I) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24208-276-15 1 in 1 CARTON 01/01/2011 1 15 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(24208-276)