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Cetacaine Anesthetic
Overview
What is Cetacaine Anesthetic?
What does Cetacaine Anesthetic look like?

What are the available doses of Cetacaine Anesthetic?
Sorry No records found.
What should I talk to my health care provider before I take Cetacaine Anesthetic?
Sorry No records found
How should I use Cetacaine Anesthetic?
Cetacaine Spray
To apply, insert the Jetco cannula (J-4) firmly onto the protruding plasticstem on the bottle and press the cannula forward to actuate the sprayvalve. The cannula may be removed and reinserted as many times asrequired for cleaning, or sterilization, and is autoclavable.
Cetacaine Liquid
*See Cetacaine Liquid Kit instructions for additional directions for applicationby Luer-lock syringe and applicator tip.
Cetacaine Gel
An appropriate pediatric dosage has not been established for CetacaineSpray, Liquid or Gel.
Dosages should be reduced in the debilitated elderly, acutely ill, andvery young patients.
Tissue need not be dried prior to application of Cetacaine. Cetacaineshould be applied directly to the site where pain control is required.Anesthesia is produced within 30 seconds with an approximateduration of 30 – 60 minutes. Each 200 mg dose of Cetacaine (Sprayresidue, Liquid or Gel) contains 28 mg of benzocaine, 4 mg of butambenand 4 mg of tetracaine HCl.
What interacts with Cetacaine Anesthetic?
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What are the warnings of Cetacaine Anesthetic?
Sorry No Records found
What are the precautions of Cetacaine Anesthetic?
Sorry No Records found
What are the side effects of Cetacaine Anesthetic?
Sorry No records found
What should I look out for while using Cetacaine Anesthetic?
Cetacaine should not be used under dentures or cotton rolls, as retentionof the active ingredients under a denture or cotton roll could possiblycause an escharotic effect. Routine precaution for the use of anytopical anesthetic should be observed when using Cetacaine.
What might happen if I take too much Cetacaine Anesthetic?
Sorry No Records found
How should I store and handle Cetacaine Anesthetic?
Store at 25°C (77°F); excursions permitted between 15°C to 30°C (59°F to 86°F). See USP Controlled Room Temperature. Do not freeze BRIVIACT injection or oral solution.Discard any unused BRIVIACT oral solution remaining after 5 months of first opening the bottle.BRIVIACT injection vials are single-dose only .Store at 25°C (77°F); excursions permitted between 15°C to 30°C (59°F to 86°F). See USP Controlled Room Temperature. Do not freeze BRIVIACT injection or oral solution.Discard any unused BRIVIACT oral solution remaining after 5 months of first opening the bottle.BRIVIACT injection vials are single-dose only .Store at 25°C (77°F); excursions permitted between 15°C to 30°C (59°F to 86°F). See USP Controlled Room Temperature. Do not freeze BRIVIACT injection or oral solution.Discard any unused BRIVIACT oral solution remaining after 5 months of first opening the bottle.BRIVIACT injection vials are single-dose only .Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017Lotensin HCT USP is available in tablets of three different strengths:Tablets of each strength are supplied in bottles that contain a desiccant and 100 tablets.The National Drug Codes for the various packages are:Tablets are oblong and scored, with “LOTENSIN HCT” on one side and appropriate number imprinted on the other side.Storage: Dispense in a tight, light-resistant container (USP). Manufactured for and Distributed by:© 2017 Validus Pharmaceuticals LLC 60024-01 August 2017
Clinical Information
Chemical Structure
No Image foundClinical Pharmacology
Non-Clinical Toxicology
Cetacaine should not be used under dentures or cotton rolls, as retentionof the active ingredients under a denture or cotton roll could possiblycause an escharotic effect. Routine precaution for the use of anytopical anesthetic should be observed when using Cetacaine.Neprilysin Inhibitors:
Patients taking concomitant neprilysin inhibitors may be at increased risk for angioedema.
Interactions Common for Both Benazepril and Hydrochlorothiazide
Dual Blockade of the Renin-Angiotensin System (RAS):
Do not coadminister aliskiren with Lotensin HCT in patients with diabetes. Avoid use of aliskiren with Lotensin HCT in patients with renal impairment (GFR < 60 mL/min).
The antihypertensive effect of benazepril and hydrochlorothiazide may be attenuated by NSAIDs.
Benazepril
Benazepril has been used concomitantly with beta-adrenergic-blocking agents, calcium-blocking agents, cimetidine, diuretics, digoxin, hydralazine, and naproxen without evidence of clinically important adverse interactions. Other ACE inhibitors have had less than additive effects with beta-adrenergic blockers, presumably because drugs of both classes lower blood pressure by inhibiting parts of the renin-angiotensin system.
Interaction studies with warfarin and acenocoumarol have failed to identify any clinically important effects of benazepril on the serum concentrations or clinical effects of these anticoagulants.
Gold:
have been reported rarely in patients on therapy with injectable gold (sodium aurothiomalate) and concomitant ACE inhibitor therapy.
Hydrochlorothiazide
Ion exchange resins:
Digitalis glycosides:
Antidiabetic agents:
Alcohol, barbiturates or narcotics:
Pressor amines:
RX Only.
Hypersensitivity Reactions
Localized allergic reactions may occur after prolonged or repeated useof any aminobenzoate anesthetic. The most common adverse reactioncaused by local anesthetics is contact dermatitis characterized by erythemaand pruritus that may progress to vesiculation and oozing. Thisoccurs most commonly in patients following prolonged self-medication,which is contraindicated. If rash, urticaria, edema, or other manifestationsof allergy develop during use, the drug should be discontinued. To minimizethe possibility of a serious allergic reaction, Cetacaine preparations should notbe applied for prolonged periods except under continual supervision. Dehydrationof the epithelium or an escharotic effect may also result from prolonged contact.
Precaution:
Reference
This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"
While we update our database periodically, we cannot guarantee it is always updated to the latest version.
Review
Professional
Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72Tips
Tips
Interactions
Interactions
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