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| Product NDC Code | 83035-8031 | ||||
|---|---|---|---|---|---|
| Drug Name | Ventiva tears plus lubricant eye drops |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | OPHTHALMIC | ||||
| Dosage Form | LIQUID | ||||
| RxCUI drug identifier | 2672491 | ||||
| Application Number | M018 | ||||
| Labeler Name | Singular Dreamer Ltd.dba True Marker | ||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Active Ingredient CARBOXYMETHYLCELLULOSE SODIUM 0.6%
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 using. Put 1 or 2 drops in the affected eye (s) as needed.
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients water, boric acid, potassium chloride, calcium chloride, magnesium chloride, sodium chlorate, chlorine dioxide, sodium borate, sodium chloride, hydrochloric acid, sodium hydroxide
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 and irritation due to dryness of the eye, for the temporary relief of discomfort due to minor irritations of the eye or to 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.Ventiva Tears Plus Lubricant Eye Drops CARBOXYMETHYLCELLULOSE SODIUM WATER BORIC ACID POTASSIUM CHLORIDE CALCIUM CHLORIDE MAGNESIUM CHLORIDE SODIUM CHLORATE SODIUM BORATE SODIUM CHLORIDE HYDROCHLORIC ACID SODIUM HYDROXIDE CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED CARBOXYMETHYLCELLULOSE
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.Product label image description image description
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.
Questions ? 1-888-811-2634
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 if this product changes color or becomes cloudy if you are sensitive to any ingredient in this product When using this product do not touch tip of container to any surface to avoid contamination replace cap after each use Stop use and ask a doctor if you experience any of the following: eye pain change in vision continued redness or irritation of the eye 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.(1-800-222-1222) 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