Dyclopro

Dyclonine Hydrochloride


Septodont Inc
Human Prescription Drug
NDC 0362-3971
Dyclopro also known as Dyclonine Hydrochloride is a human prescription drug labeled by 'Septodont Inc'. National Drug Code (NDC) number for Dyclopro is 0362-3971. This drug is available in dosage form of Solution. The names of the active, medicinal ingredients in Dyclopro drug includes Dyclonine Hydrochloride - 5 mg/mL . The currest status of Dyclopro drug is Active.

Drug Information:

Drug NDC: 0362-3971
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Dyclopro
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Prescription Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Dyclonine Hydrochloride
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Septodont Inc
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Solution
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:DYCLONINE HYDROCHLORIDE - 5 mg/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:TOPICAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: ANDA
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Marketing Start Date: 01 Sep, 2019
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 01 Jan, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Application Number: ANDA200480
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Septodont Inc
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
RxCUI:1048281
2199132
The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
UNII:ZEC193879Q
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
0362-3971-051 BOTTLE in 1 BOTTLE (0362-3971-05) / 30 mL in 1 BOTTLE01 Sep, 2019N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Product Elements:

Dyclopro dyclonine hydrochloride dyclonine hydrochloride dyclonine chlorobutanol sodium chloride hydrochloric acid water

Indications and Usage:

Indications and usage: dyclonine hcl topical solution, usp is indicated for anesthetizing accessible mucous membranes (e.g., the mouth, pharynx, larynx, trachea, esophagus, and urethra) prior to various endoscopic procedures. dyclonine hcl topical solution, usp, 0.5% topical anesthetic may also be used to block the gag reflex, to relieve the pain of oral ulcers or stomatitis and to relieve pain associated with ano-genital lesions.

Warnings:

Warnings: in order to manage possible adverse reactions, resuscitative equipment, oxygen and other resuscitative drugs should be immediately available whenever local anesthetic agents, such as dyclonine, are administered to mucous membranes. dyclonine hcl topical solution, usp should not be injected into tissue or used in the eyes because of highly irritant properties. dyclonine hcl topical solution, usp should be used with extreme caution in the presence of sepsis or severely traumatized mucosa in the area of application since under such conditions there is the potential for rapid systemic absorption.

Dosage and Administration:

Dosage and administration: as with all local anesthetics, the dosage varies and depends upon the area to be anesthetized, vascularity of the tissues, individual tolerance and the technique of anesthesia. the lowest dosage needed to provide effective anesthesia should be administered. a maximum dose of 30 ml of dyclonine hcl topical solution, usp 1% topical anesthetic (300 mg of dyclonine hcl) may be used, although satisfactory anesthesia is usually produced within the range of 4 to 20 ml. for specific techniques and procedures refer to standard textbooks. although as much as 300 mg of dyclonine hcl topical solution usp (as a 1% solution) have been tolerated, this dosage as a 0.5% solution has not been administered primarily because satisfactory anesthesia in endoscopic procedures can usually be produced by lesser amounts. for specific techniques for endoscopic procedures refer to standard textbooks. dyclonine hcl topical solution, usp can be used for a period of 7 days after open.

Contraindications:

Contraindications: dyclonine hcl topical solution, usp is contraindicated in patients known to be hypersensitive (allergic) to the local anesthetic or to other components of dyclonine hcl topical solution, usp .

Adverse Reactions:

Adverse reactions: adverse experiences following the administration of dyclonine are similar in nature to those observed with other local anesthetic agents. these adverse experiences are, in general, dose-related and may result from high plasma levels caused by excessive dosage or rapid absorption, or may result from a hypersensitivity, idiosyncrasy or diminished tolerance on the part of the patient. serious adverse experiences are generally systemic in nature. the following types are those most commonly reported: central nervous system: cns manifestations are excitatory and/or depressant and may be characterized by lightheadedness, nervousness, apprehension, euphoria, confusion, dizziness, drowsiness, tinnitus, blurred or double vision, vomiting, sensations of heat, cold or numbness, twitching, tremors, convulsions, unconsciousness, respiratory depression and arrest. the excitatory manifestations may be very brief or may not occur at all, in which case the first manifestation of toxic
ity may be drowsiness merging into unconsciousness and respiratory arrest. drowsiness following the administration of dyclonine is usually an early sign of a high blood level of the drug and may occur as a consequence of rapid absorption. cardiovascular system: cardiovascular manifestations are usually depressant and are characterized by bradycardia, hypotension, and cardiovascular collapse, which may lead to cardiac arrest. allergic: allergic reactions are characterized by cutaneous lesions, urticaria, edema or anaphylactoid reactions. allergic reactions may occur as a result of sensitivity either to the local anesthetic agent or to the other ingredients used in this formulation. allergic reactions, if they occur, should be managed by conventional means. the detection of sensitivity by skin testing is of doubtful value. local reactions include irritation, stinging, urethritis with and without bleeding.

Use in Pregnancy:

Pregnancy: teratogenic effects: pregnancy category c. animal reproduction studies have not been conducted with dyclonine hydrochloride. it is also not known whether dyclonine hydrochloride can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. dyclonine hydrochloride should be given to pregnant women only if clearly needed.

Pediatric Use:

Pediatric use: safety and effectiveness in children under the age of 12 have not been established.

Overdosage:

Overdosage: acute emergencies from local anesthetics are generally related to high plasma levels encountered during therapeutic use of local anesthetics. (see adverse reactions, warnings and precautions ). management of local anesthetic emergencies: the first consideration is prevention, best accomplished by careful and constant monitoring of cardiovascular and respiratory vital signs and the patient’s state of consciousness after each local anesthetic administration. the first step in the management of convulsions consists of immediate attention to the maintenance of a patent airway and assisted or controlled ventilation with oxygen and a delivery system capable of permitting immediate positive airway pressure by mask. immediately after the institution of these ventilatory measures, the adequacy of the circulation should be evaluated, keeping in mind that drugs used to treat convulsions sometimes depress the circulation when administered intravenously. should convulsions persist despite adequate respiratory support, and if the status of the circulation permits, small increments of an ultra-short acting barbiturate (such as thiopental or thiamylal) or a benzodiazepine (such as diazepam) may be administered intravenously. the clinician should be familiar, prior to use of local anesthetics, with these anticonvulsant drugs. supportive treatment of circulatory depression may require administration of intravenous fluids and, when appropriate, a vasopressor as directed by the clinical situation (e.g., ephedrine). if not treated immediately, both convulsions and cardiovascular depression can result in hypoxia, acidosis, bradycardia, arrhythmias and cardiac arrest. if cardiac arrest should occur, standard cardiopulmonary resuscitative measures should be instituted. the median lethal dose (ld 50 ) of dyclonine hcl topical solution, usp administered orally to female rats is 176 mg/kg and 90 mg/kg in female mice. intraperitoneally the ld 50 in female rats is 31 mg/kg and 43 mg/kg in female mice.

Description:

Description: dyclopro (dyclonine hydrochloride topical solution, usp, 0.5% and 1%) topical anesthetics contain a local anesthetic agent and are administered topically. see indications for specific uses. dyclopro (dyclonine hydrochloride topical solution, usp, 0.5% and 1%) contain dyclonine hcl, which is chemically designated as 4’-butoxy-3-piperidinopropiophenone hcl. dyclonine hcl is a white crystalline powder that is sparingly soluble in water and has the following structural formula: structural formula

Clinical Pharmacology:

Clinical pharmacology: dyclonine hcl topical solution, usp effects surface anesthesia when applied topically to mucous membranes. effective anesthesia varies with different patients, but usually occurs from 2 to 10 minutes after application and persists for approximately 30 minutes.

Carcinogenesis and Mutagenesis and Impairment of Fertility:

Carcinogenesis, mutagenesis, impairment of fertility: long-term animal studies have not been performed to evaluate the potential mutagenic or carcinogenic potential of dyclonine hydrochloride. likewise, animal studies to characterize the potential effects of dyclonine hydrochloride on fertility have not been completed.

How Supplied:

How supplied: clear and colorless sterile solution, in one fluid ounce bottles. multi dose dyclonine hcl topical solution 0.5% (ndc 0362-3971-05) dyclonine hcl topical solution 1% (ndc 0362-3918-10). store at 20° to 25°c (68° to 77°f) [see usp controlled room temperature]. keep upright and preserve in tight and light-resistant container. avoid excessive heat (temperatures above 40ºc [104ºf]). subject to damage by freezing.

Information for Patients:

Information for patients: when topical anesthetics are used in the mouth or throat, the patient should be aware that the production of topical anesthesia may impair swallowing and thus enhance the danger of aspiration. for this reason, food should not be ingested for 60 minutes following use of local anesthetic preparations in the mouth or throat area. this is particularly important in children because of their frequency of eating. numbness of the tongue or buccal mucosa may increase the danger of biting trauma. when dyclonine hcl topical solution, usp is used to relieve the pain of oral ulcers or stomatitis which interferes with eating, patients should be warned about the risk of biting trauma before they accept this treatment; caution should be exercised in selecting food and eating. following other uses in the mouth and throat area, food and/or chewing gum should not be used while the area is anesthetized.

Package Label Principal Display Panel:

Principal display panel - carton - 0.5% ndc 0362-3971-05 dyclopro (dyclonine hydrochloride topical solution, usp, 0.5%) topical anesthetic 1fl.oz. (30ml) not for injection not for use in the eyes. rx only multi dose manufactured for septodont, inc. 205 granite run dr., suite 150, lancaster, pa, usa 17601 by novocol pharmaceutical of canada, inc. ontario, canada n1r 6x3 dyclopro_dyclonine 0.5 (us) box


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