Label: MURO 128- sodium chloride ointment
- NDC Code(s): 24208-385-01, 24208-385-55, 24208-385-56
- Packager: Bausch & Lomb Incorporated
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated September 25, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
-
Warnings
For external use only
Do not use
except under the advice and supervision of a doctor.When using this product
- it may cause temporary burning and irritation
- replace cap after use
- to avoid contamination, do not touch tip of container to any surface
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
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Other information
- store at 15-25 °C (59-77 °F)
- keep tightly closed
- DO NOT FREEZE
- see crimp of tube or carton for Lot Number and Expiration Date
- do not use if difficult to dispense or visible particles are seen in the product
- serious side effects associated with use of the product may be reported to the phone number provided below
- Inactive ingredients
- Questions or comments?
- Package/Label Principal Display Panel
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INGREDIENTS AND APPEARANCE
MURO 128
sodium chloride ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24208-385 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 g Inactive Ingredients Ingredient Name Strength LANOLIN (UNII: 7EV65EAW6H) WATER (UNII: 059QF0KO0R) PETROLATUM (UNII: 4T6H12BN9U) MINERAL OIL (UNII: T5L8T28FGP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24208-385-55 1 in 1 CARTON 01/01/2011 1 3.5 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:24208-385-56 2 in 1 CARTON 01/01/2011 2 3.5 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:24208-385-01 1 in 1 CARTON 01/01/2011 3 1 g in 1 TUBE; 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(24208-385)