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| Product NDC Code | 71331-113 | ||||
|---|---|---|---|---|---|
| Drug Name | Nupharmisto |
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| Type | Brand | ||||
| Pharm Class | Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE] |
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| Active Ingredients |
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| Route | TOPICAL | ||||
| Dosage Form | CREAM | ||||
| RxCUI drug identifier | 2675779 | ||||
| Application Number | M015 | ||||
| Labeler Name | Orange Lab, Inc | ||||
| 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.Drug Facts Drug facts - active
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.Active ingredient and directions Active Ingredient directions
Inactive ingredient
A list of inactive, non-medicinal ingredients in a drug product.Inactive Ingredients Inactive ingredients
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.Usage section Usage
Purpose
Information about the drug product’s indications for use.Purpose Local Anesthetic Uses
Spl product data elements
Usually a list of ingredients in a drug product.Nupharmisto Lidocaine ALLANTOIN ARNICA MONTANA FLOWER ETHYLHEXYLGLYCERIN WATER PROPYLENE GLYCOL EMU OIL TRIDECETH-6 ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) HYDROGENATED POLYDECENE (1500 CST) SUNFLOWER OIL UNSAPONIFIABLES ETHYLHEXYL PALMITATE PHENOXYETHANOL SODIUM POLYACRYLATE (8000 MW) .ALPHA.-TOCOPHEROL ACETATE DIMETHYL ISOSORBIDE MENTHOL MENTHOL LIDOCAINE LIDOCAINE EDETATE SODIUM
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 Images Label 01 Label 02
Instructions for use
Information about safe handling and use of the drug product.Directions for use Directions
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 keep out of reach of children
Other safety information
Information about safe use and handling of the product that may not have been specified in another field.How to use it correctly? How to use it correctly?
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 pregnant
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 when using this product
Storage and handling
Information about safe storage and handling of the drug product.Other information : storage Other information
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 Warnings
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