Topical Application definition

Topical Application means the treatment of disease by delivery in a topical dosage form to the outer surface of the diseased area for dermatologic and ophthalmic administration.
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Topical Application means application of any formulation of a compound directly to the skin, wherein such topical application has its therapeutic effect directly on the skin or its components where applied and has minimal or no systemic effect.
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Examples of Topical Application in a sentence

  • When visiting a physician with your infant, DDWA will reimburse the physician as a Non-Participating Provider, on your behalf for Oral Evaluation and Topical Application of Fluoride services performed.

  • Reimbursement will be based on 100 percent of the applicable Non-Participating Provider fee for either Oral Evaluation or Topical Application of Fluoride, or both, depending on actual services provided.Please see the “Benefits Covered by Your Plan” section of this booklet for any other limitations.

  • We reviewed all 15 scenarios and determined the ones that could best benefit from the potential response capabilities of community health call centers.

  • The following warning statement: “For Topical Application – Do Not Eat or Smoke.”E.

  • Leukemia or HIV induced gingivitis.Fluoride Treatments (Topical Application and Fluoride Varnish).Topical Fluoride Treatments are limited to three (3) treatments in a 12 consecutive month period for members through age 18.

  • All necessary procedures to prevent the occurrence of oral disease, including: Cleaning and Scaling Topical Application of Fluoride Space Services All necessary procedures for extractions and other surgical procedures normally performed by a dentist.

  • After the specialty code, FC-Fluoride Certification, is added to the provider’s file, the provider will be able to bill for procedure code D1206, Topical Application of Fluoride Varnish.Providers must check the Supplemental Eligibility Screen to verify that topical fluoride varnish benefit of two (2) per State Fiscal Year (SFY) has not been exhausted.

  • Table 3: Summary of plasma dapsone PK parameters following dosing on Day 28PK parameter Figure 1: Mean Plasma Concentrations of Dapsone (ng/mL) on Day 28 Following Once Daily Topical Application of dapsone gel, 7.5% (Formulation 11080X) Note: This trial also include 2 additional treatment arms of other dapsone gel, 7.5% formulations, namely formulations 11078X and 11079X; however, these are pilot formulations that were not developed and they are not discussed further here.

  • Topical Application of Cream-emulsified CD86 siRNA Ameliorates Allergic Skin Disease by Targeting Cutaneous Dendritic Cells.

  • Topical Application of Fluoride Varnish Fluoride varnish may be the preferred delivery method for individuals receiving head and neck radiation therapy and/or moderate to high caries risk individuals with a medical or cognitive impairment Xerostomia.

Related to Topical Application

  • Practical application means to manufacture in the case of a composition or product, to practice in the case of a process or method, or to operate in the case of a machine or system; and, in each case, under such conditions as to establish that the invention is being utilized and that its benefits are, to the extent permitted by law or government regulations, available to the public on reasonable terms.

  • Approval Application means a BLA, NDA or similar application or submission for a Product filed with a Regulatory Authority in a country or group of countries to obtain marketing approval for a biological or pharmaceutical product in that country or group of countries.

  • Marketing Approval Application or “MAA” means a New Drug Application (or its equivalent), as defined in the U.S. Food, Drug and Cosmetic Act and the regulations promulgated thereunder, or any corresponding or similar application, registration or certification in any country.

  • Regulatory Approval Application means any application submitted to an appropriate Regulatory Authority seeking any Regulatory Approval.

  • Initial application means the Application first provided to MFA on or before an Application Deadline to request an allocation of Tax Credits.

  • Development Application means the development application identified in Item 5 of Schedule 1 and includes all plans, reports models, photomontages, material boards (as amended supplemented) submitted to the consent authority before the determination of that Development Application.

  • Commercial applicator means any person, unless exempted in I(4) hereunder, whether or not the person is a private applicator with respect to some uses, who:

  • Renewal Application means a document used to collect pertinent data for renewal of permits

  • Marketing Authorization Application or “MAA” means an application for Regulatory Approval in a country, territory or possession.

  • Drug Approval Application means an application for Regulatory Approval required before commercial sale or use of a Product as a drug in a regulatory jurisdiction.

  • international application means an application filed under this Treaty;

  • SAP Application(s) means all Packages (i.e. all Software and Third Party Software) licensed under the Agreement and/or SAP cloud services for which Customer has a valid subscription, excluding User Interfaces for ERP, SAP Technology Solutions and all database Packages.

  • Civil Aeronautical Product means any civil aircraft, aircraft engine, or propeller or subassembly, appliance, material, part, or component to be installed thereon.

  • Commercial Product means any such product as defined in FAR 2.101.

  • Licensed Application means an Application that (a) meets and complies with all of the Documentation and Program Requirements, and (b) has been selected and digitally signed by Apple for distribution, and includes any additional permitted functionality, content or services provided by You from within an Application using the In-App Purchase API.

  • Planning Application means the application for [outline/full] planning permission dated [ ] bearing the Council’s reference number [ ];

  • Patent Application means an application for patent protection for a CRADA Subject Invention with the United States Patent and Trademark Office (“U.S.P.T.O.”) or the corresponding patent-issuing authority of another nation.

  • Licensed Product means a product, method or service in the Licensed Field of Use, the making, having made, using, importing or selling of which, absent this license, infringes, induces infringement, or contributes to infringement of a Licensed Patent.

  • Collaboration Product means a pharmaceutical product containing or comprising Compound in any dosage form alone, or in combination with, one or more other pharmaceutically active ingredients, and any and all Improvements thereto.

  • Tobacco product means any substance containing tobacco leaf, including but not limited to, cigarettes, cigars, pipe tobacco, hookah tobacco, snuff, chewing tobacco, dipping tobacco, bidis, blunts, clove cigarettes, or any other preparation of tobacco; and any product or formulation of matter containing biologically active amounts of nicotine that is manufactured, sold, offered for sale, or otherwise distributed with the expectation that the product or matter will be introduced into the human body by inhalation; but does not include any cessation product specifically approved by the U.S. Food and Drug Administration for use in treating nicotine or tobacco dependence.

  • Third Party Applications means online, Web-based applications and offline software products that are provided by third parties and are identified as third-party applications, including but not limited to those listed on the AppExchange and the Reseller Application.

  • WTO GPA country end product means an article that—

  • Mobile Application means a specialized software program downloaded onto a wireless communication device.

  • Biological product means a virus, therapeutic serum, toxin, antitoxin, vaccine, blood, blood component or derivative, allergenic product, protein other than a chemically synthesized polypeptide, or analogous product, or arsphenamine or any derivative of arsphenamine or any other trivalent organic arsenic compound, applicable to the prevention, treatment, or cure of a disease or condition of human beings.

  • medicinal product means any substance or combination of substances presented for treating or preventing disease in human beings or animals and any substance or combination of substances which may be administered to human beings or animals with a view to making a medical diagnosis or to restoring, correcting or modifying physiological functions in humans or in animals;

  • ANDA means an Abbreviated New Drug Application filed with the FDA pursuant to its rules and regulations.