SODIUM CHLORIDE- sodium chloride solution/ drops 
Rite Aid Corporation

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 Facts

Active ingredient

Sodium Chloride 5%

Purpose

Hypertonicity Agent

Use

Warnings

Do not use

  • this product except under the advice and supervision of a doctor.
  • if imprinted seal is broken or missing.
  • if solution changes color or becomes cloudy.

When using this product

  • temporary burning and irritation upon being instilled into eye may occur.
  • to avoid contamination, do not touch tip of container to any surface.
  • replace cap after each use.

Stop use and ask a doctor if

  • you experience eye pain.
  • you experience changes in vision.
  • redness or irritation of the eye continues
  • condition worsens or persists.

Keep out of reach of children.

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

Directions

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

Other information

Inactive ingredients

Boric Acid, Hypromellose 2906, Methylparaben 0.23 mg (0.023%), Propylparaben 0.1 mg (0.01%), Propylene Glycol, Sodium Borate, Sodium Hydroxide and/or Hydrochloric Acid to adjust pH (6.0 to 8.0), and Purified Water USP.

Questions

call 1-800-579-8327

Principal Display Panel Text for Container Label:

RITE
AID®
PHARMACY

eye care
ophthalmic
solution
sodium chloride USP 5%
hypertonicity
eye drops
Sterile
0.5 FL OZ (15 mL)

Principal Display Panel Text for Container Label:

Principal Display Panel Text for Carton Label:

RITE                      Compare to the active
AID®                     ingredient in Muro-128®*
PHARMACY         NDC 11822-5458-1
eye care
ophthalmic
solution
sodium chloride USP 5%
hypertonicity
eye drops
temporary relief
of corneal edema
doctor recommended
Sterile
0.5 FL OZ (15 mL)

Principal Display Panel Text for Carton Label:
SODIUM CHLORIDE 
sodium chloride solution/ drops
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11822-5458
Route of AdministrationOPHTHALMIC
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Chloride (UNII: 451W47IQ8X) (Sodium Cation - UNII:LYR4M0NH37) Sodium Chloride50 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Boric Acid (UNII: R57ZHV85D4)  
Hypromelloses (UNII: 3NXW29V3WO)  
Propylene Glycol (UNII: 6DC9Q167V3)  
Sodium Borate (UNII: 91MBZ8H3QO)  
Sodium Hydroxide (UNII: 55X04QC32I)  
Hydrochloric Acid (UNII: QTT17582CB)  
Water (UNII: 059QF0KO0R)  
Methylparaben (UNII: A2I8C7HI9T)  
Propylparaben (UNII: Z8IX2SC1OH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11822-5458-11 in 1 CARTON02/21/2013
115 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34902/21/2013
Labeler - Rite Aid Corporation (014578892)
Registrant - Akorn Operating Company LLC (117693100)
Establishment
NameAddressID/FEIBusiness Operations
Akorn117696790PACK(11822-5458) , LABEL(11822-5458)
Establishment
NameAddressID/FEIBusiness Operations
Akorn117696832MANUFACTURE(11822-5458) , ANALYSIS(11822-5458) , STERILIZE(11822-5458)

Revised: 1/2022
Document Id: 19400574-c997-475d-b454-a1d3a213948d
Set id: c7acc338-2b84-4929-9b23-3abc35a3edcd
Version: 4
Effective Time: 20220127
 
Rite Aid Corporation