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NDC 24208-0277-15 Muro 128 50 mg/mL Details

Muro 128 50 mg/mL

Muro 128 is a OPHTHALMIC SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by Bausch & Lomb Incorporated. The primary component is SODIUM CHLORIDE.

Product Information

NDC	24208-0277
Product ID	24208-277_c9211ab1-d0af-4298-bfc1-9840cc131903
Associated GPIs	86804030102005
GCN Sequence Number	007739
GCN Sequence Number Description	sodium chloride DROPS 5 % OPHTHALMIC
HIC3	Q6A
HIC3 Description	OPHTHALMIC PREPARATIONS, MISCELLANEOUS
GCN	31923
HICL Sequence Number	003389
HICL Sequence Number Description	SODIUM CHLORIDE
Brand/Generic	Brand
Proprietary Name	Muro 128
Proprietary Name Suffix	n/a
Non-Proprietary Name	sodium chloride
Product Type	HUMAN OTC DRUG
Dosage Form	SOLUTION
Route	OPHTHALMIC
Active Ingredient Strength	50
Active Ingredient Units	mg/mL
Substance Name	SODIUM CHLORIDE
Labeler Name	Bausch & Lomb Incorporated
Pharmaceutical Class	Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]
DEA Schedule	n/a
Marketing Category	OTC MONOGRAPH FINAL
Application Number	part349
Listing Certified Through	2024-12-31

Package

Package Images

NDC 24208-0277-15 (24208027715)

Pricing Information	N/A
NDC Package Code	24208-277-15
Billing NDC	24208027715
Package	1 BOTTLE in 1 CARTON (24208-277-15) / 15 mL in 1 BOTTLE
Marketing Start Date	2011-01-01
NDC Exclude Flag	N

Standard Product Labeling (SPL)/Prescribing Information SPL 454f337e-d897-46de-ab05-1c543a33061c Details

Drug Facts

Active ingredient

Sodium chloride 5%

Purpose

Hypertonicity agent

Uses

temporary relief of corneal edema

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.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

: Instill 1 or 2 drops in the affected eye(s) every 3 or 4 hours, or as directed by a doctor.

Other information

•: store upright at 15–25 °C (59–77 °F)
•: keep tightly closed
•: serious side effects associated with use of the product may be reported to the phone number provided below

Inactive ingredients

boric acid, hypromellose, methylparaben, propylene glycol, propylparaben, purified water, sodium borate. Hydrochloric acid and/or sodium hydroxide may be added to adjust pH.

Questions or comments?

[telephone icon] Call1-800-553-5340

Muro 128 is a trademark of Bausch & Lomb Incorporated or its affiliates.

Marketed by:

Bausch & Lomb Americas Inc.

Bridgewater, NJ 08807 USA

9756601

AB15611

Package/Label Principal Display Panel – Muro 128 15 mL

BAUSCH + LOMB

NDC 24208-277-15

Muro 128®

sodium chloride hypertonicity

ophthalmic solution, 5%

SOLUTION

Temporary Relief

of Corneal Edema

STERILE

1/2 FL OZ (15 mL)

INGREDIENTS AND APPEARANCE

MURO 128

sodium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:24208-277
Route of Administration	OPHTHALMIC

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
SODIUM CHLORIDE (UNII: 451W47IQ8X) (SODIUM CATION - UNII:LYR4M0NH37)	SODIUM CHLORIDE	50 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
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)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
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 Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part349	01/01/2011

Labeler - Bausch & Lomb Incorporated (196603781)

Name	Address	ID/FEI	Business Operations
Establishment
Bausch & Lomb Incorporated		079587625	MANUFACTURE(24208-277)

Revised: 5/2022

Document Id: c9211ab1-d0af-4298-bfc1-9840cc131903

Set id: 454f337e-d897-46de-ab05-1c543a33061c

Version: 7

Effective Time: 20220525