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| Product NDC Code | 84938-001 | ||||
|---|---|---|---|---|---|
| Drug Name | Eye drops |
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| Type | Brand | ||||
| Active Ingredients |
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| Route | OPHTHALMIC | ||||
| Dosage Form | LIQUID | ||||
| RxCUI drug identifier | 1547948 | ||||
| Application Number | M018 | ||||
| Labeler Name | Foshan Sugar Max Cosmetics CO.,Ltd | ||||
| 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.Carboxymethylcellulose sodium 0.25%
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 Instilllor 2 drops in the affected eye(s) asneeded
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.calciumchloride Dequest magnesium chloride potassium chloride purified water sodium bicarbonate sodium chloride sodium perborate sodium phosphate
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, anddiscomfort due to dryness of the eye or exposure towind or sun. May be used as a protectant against further irritation.
Purpose
Information about the drug product’s indications for use.Eye lubricant
Spl product data elements
Usually a list of ingredients in a drug product.EYE DROPS Carboxymethylcellulose sodium CALCIUM CHLORIDE ANHYDROUS SODIUM CHLORIDE POTASSIUM CHLORIDE WATER SODIUM PERBORATE CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED CARBOXYMETHYLCELLULOSE SODIUM BICARBONATE SODIUM PHOSPHATE AMINOTRIS(METHYLENEPHOSPHONIC ACID) 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.label
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.EYE DROPS
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. lf swallowed, get medicalhelp or contact a Poison Control Center 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 experience eye pain,changes in vision, continued redness or irritation of theeye, or if the condition worsens or persists for more than72 hours.
Storage and handling
Information about safe storage and handling of the drug product.Use only if tape seals on top and bottom flaps areintact. Use before expiration date marked on container. Discard 90 days after opening.
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.For external use only. To avoid contamination, do not touch tip of container toany surface. Replace cap after using. lf solution changes color or becomes cloudy, do not use.
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