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Base laboratories corneal flow hypertonicity ophthalmic eye - Medication Information

Product NDC Code 80327-011
Drug Name

Base laboratories corneal flow hypertonicity ophthalmic eye

Type Brand
Active Ingredients
Sodium chloride 30 mg/g
Route TOPICAL
Dosage Form OINTMENT
RxCUI drug identifier 1298435
Application Number M018
Labeler Name Joonem LLC
Packages
Package NDC Code Description
80327-011-00 3 tube in 1 carton (80327-011-00) / 5 g in 1 tube
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Sodium chloride 3% Purpose Hypertonicity agent

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions Pull down the lower lid of the affected eye Apply a small amount (1/4 inch) of ointment to the inside of eyelid Apply every 3 to 4 hours or as directed by a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water, Glycerin, Propylene Glycol, Squalane, Sodium Hyaluronate, Dimethicone, Tocopheryl Acetate, Carnosine, Butylene Glycol, Phenoxyethanol, Chlorphenesin, Ubiquinone

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses: Temporary relief of corneal edema

Purpose

Information about the drug product’s indications for use.
Purpose Hypertonicity agent

Spl product data elements

Usually a list of ingredients in a drug product.
Base Laboratories Corneal Flow Hypertonicity Ophthalmic Eye SODIUM CHLORIDE WATER GLYCERIN PROPYLENE GLYCOL SQUALANE HYALURONATE SODIUM DIMETHICONE .ALPHA.-TOCOPHEROL ACETATE CARNOSINE BUTYLENE GLYCOL PHENOXYETHANOL CHLORPHENESIN UBIDECARENONE SODIUM CHLORIDE CHLORIDE ION

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Package Labeling: Label0

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts Other information Store at 15-25C (59-77F) Keep tightly closed Do not Freeze Do not use if difficult to dispense or visible particles are seen in the product Side effects associated with this product may be reported to the email address below

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use Except under the advice and supervision of a doctor

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or comments? [email protected]

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
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

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product It may cause temporary burning and irritation Replace cap after use To avoid contamination, do not touch top of container to any surface

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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 top 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. If swallowed, get medical help or contact a Poison Control Center right away.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API

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