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Product NDC Code | 11673-126 | ||||
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Drug Name | Up and up lubricant |
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Type | Brand | ||||
Active Ingredients |
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Route | OPHTHALMIC | ||||
Dosage Form | SOLUTION/ DROPS | ||||
RxCUI drug identifier | 1188426 | ||||
Application Number | part349 | ||||
Labeler Name | Target Corporation | ||||
Packages |
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Active ingredient
A list of the active, medicinal ingredients in the drug product.Active ingredient Purpose Carboxymethylcellulose sodium 0.5%................Eye lubricant
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.Distributed by Target Corporation Made in South Korea
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive ingredients calcium chloride, hydrochloric acid, magnesium chloride, potassium chloride. purified water, sodium chloride, sodium hydroxide, sodium lactate
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.Directions to open, twist and pull tab to remove instill 1 or 2 drops in the affected eye(s) as needed and discard container children under 6 years of age: ask a doctor
Purpose
Information about the drug product’s indications for 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
Spl product data elements
Usually a list of ingredients in a drug product.Up and Up Lubricant Carboxymethylcellulose Sodium CARBOXYMETHYLCELLULOSE SODIUM CARBOXYMETHYLCELLULOSE CALCIUM CHLORIDE HYDROCHLORIC ACID WATER SODIUM HYDROXIDE SODIUM LACTATE SODIUM CHLORIDE POTASSIUM CHLORIDE MAGNESIUM CHLORIDE
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.675.1
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 children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.
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 you feel eye pain changes in vision occur continued redness or irritation of the eye lasts condition worsens or lasts more than 72 hours
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 do not touch tip of container to any surface to avoid contamination do not reuse once opened, discard do not use if this solution changes color or becomes cloudy
Pregnancy or breast feeding
Pregnancy or Breast feedingIf pregnant or breast-feeding, ask a health professional before use.
Storage and handling
Information about safe storage and handling of the drug product.Other information store between 15-30°C (59-86°F) protect from light
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
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