Your browser does not support JavaScript! SODIUM CHLORIDE OINTMENT [WALGREENS]
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RxNorm Names

SODIUM CHLORIDE ointment
[Walgreens]


Category DEA Schedule Marketing Status
HUMAN OTC DRUG LABEL OTC monograph final
NOTE: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 Label Sections

Drug Facts

Active ingredient

Sodium Chloride 5%

Purpose

Hypertonicity agent

Use

For temporary relief of corneal edema.

Warnings

  • Do not use this product except under the advice and supervision of a doctor.
  • Do not use if bottom ridge of tube cap is exposed.
  • To avoid contamination, do not touch tip of container to any surface.
  • Replace cap after using.
  • May cause temporary burning and irritation upon application into the eye.

Stop use and ask a doctor if you experience eye pain, changes in vision, continued redress or irritation of the eye, or if the condition worsens or persists for more than 72 hours.

Keep out of reach of children.

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

Directions

Apply small amount (one-fourth inch) to the inside of affected eye(s) every 3 to 4 hours, or as directed by a doctor.

Other Information

  • Store at 20° to 25° C (68° to 77°F) [see USP Controlled Room Temperature].
  • Store away from heat.
  • Protect from freeing.
  • Keep tightly dosed.
  • See crimp for Control Number and Expiration Date.
  • RETAIN THIS CARTON FOR FUTURE REFERENCE.

Inactive ingredients

Mineral Oil, Modified Lanolin, Purified Water and White Petrolatum.

Questions or comments?

1-800-579-8327

Principal Display Panel Text for Container Label:

STERILE Well at

Sodium Chloride Walgreens

Ophthalmic Ointment NDC 0363-9050-00

USP, 5% NET WT 3.5 g (1/8 oz.)

Hypertonicity Eye Ointment

FOR OPHTHALMIC USE ONLY

Principal Display Panel Text for Container Label

Principal Display Panel Text for Carton Label:

STERILE NEW

Sodium Chloride Well at

Ophthalmic Ointment Walgreens NDC 0363-9050-00

USP, 5% WALGREENS PHARMACIST RECOMMENDED≠

Hypertonicity Eye Ointment

Compare to Muro 128®

NET WT 3.5 g (1/8 oz.) Ointment active ingredient#

Principal Display Panel Text for Carton Label
SODIUM CHLORIDE 
sodium chloride ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9050
Route of AdministrationOPHTHALMICDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Chloride (Sodium Cation) Sodium Chloride50 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Mineral Oil 
Lanolin 
Water 
Petrolatum 
Packaging
#Item CodePackage Description
1NDC:0363-9050-001 in 1 CARTON
13.5 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34902/12/2013
Labeler - Walgreens (008965063)
Registrant - Akorn, Inc. (062649876)
Establishment
NameAddressID/FEIBusiness Operations
Akorn, Inc603980319MANUFACTURE(0363-9050), ANALYSIS(0363-9050), STERILIZE(0363-9050), PACK(0363-9050), LABEL(0363-9050)

Revised: 02/2013
Document Id: b0ad8f9e-4849-4732-ba2c-fffc803bac38
Set id: 72342206-7b82-46e9-95e0-1e1cea8678a3
Version: 1
Effective Time: 20130212
 
Walgreens

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