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Polyvinyl alcohol - Medication Information

Product NDC Code 50090-7119
Drug Name

Polyvinyl alcohol

Type Generic
Active Ingredients
Polyvinyl alcohol 14 mg/ml
Route OPHTHALMIC
Dosage Form SOLUTION/ DROPS
RxCUI drug identifier 142004
Application Number M018
Labeler Name A-S Medication Solutions
Packages
Package NDC Code Description
50090-7119-0 15 ml in 1 bottle (50090-7119-0)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Polyvinyl Alcohol 1.4%

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 Shake well before use instill 1 to 2 drops in the affected eye(s) as needed

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients dibasic sodium phosphate, edetate disodium, monobasic sodium phosphate, purified water, sodium chloride. Phosphoric acid and/or sodium hydroxide may be added to adjust pH. PRESERVATIVE ADDED: benzalkonium chloride 0.01%

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 for the temporary relief of burning, irritation and discomfort due to dryness of the eye or exposure to wind or sun may be used as a protectant against further irritation

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Polyvinyl Alcohol Polyvinyl Alcohol SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM EDETATE DISODIUM SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM SODIUM CHLORIDE WATER BENZALKONIUM CHLORIDE POLYVINYL ALCOHOL POLYVINYL ALCOHOL

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.
Polyvinyl Alcohol Label Image

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.
Other information Store at room temperature 15-30C (59-86C) Do No Use if imprinted seal on cap is torn, broken or missing Discard 90 days after opening Retain outer carton for full product information

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 (1-800-222-1222)

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions ? Call 1-855-361-3993 Distributed by: AvKARE Pulaski, TN 38478 www.avkare.com Rev. 12/2022 AV 12/2022

How supplied

Information about the available dosage forms to which the labeling applies, and for which the manufacturer or distributor is responsible. This field ordinarily includes the strength of the dosage form (in metric units), the units in which the dosage form is available for prescribing, appropriate information to facilitate identification of the dosage forms (such as shape, color, coating, scoring, and National Drug Code), and special handling and storage condition information.
HOW SUPPLIED Product: 50090-7119 NDC: 50090-7119-0 15 mL in a BOTTLE

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 Do not use if solution changes color or becomes cloudy When using this product Avoid contamination, do not touch tip of container to any surface. Replace cap after use Stop use and ask a doctor if you experience eye pain, changes in vision, continued redness or irritation of the eye the condition worsens or persists for more than 72 hours

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