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Side Effects & Adverse Reactions
For external use only.
do not use while smoking or near heat or flame.
- in the eyes
- over large areas of the body
- longer than 1 week unless directed by a doctor
- on infected areas or wounds that are draining
- with other first aid products such as lotions and creams
- over sutures
- on mucous membranes
- deep puncture wounds
- deep cuts
- animal bites
- serious bleeding
- diabetes
- poor circulation
- serious burns
- do not sotre at temperaure above 120oF
Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.
- conditions persists or gets worse
- infection occurs
If swallowed, get medical help or call a Poison Control Center right away.
- in the eyes
- over large areas of the body
- longer than 1 week unless directed by a doctor
- on infected areas or wounds that are draining
- with other first aid products such as lotions and creams
- over sutures
- on mucous membranes
- deep puncture wounds
- deep cuts
- animal bites
- serious bleeding
- diabetes
- poor circulation
- serious burns
- conditions persists or gets worse
- infection occurs
Legal Issues
There is currently no legal information available for this drug.
FDA Safety Alerts
There are currently no FDA safety alerts available for this drug.
Manufacturer Warnings
There is currently no manufacturer warning information available for this drug.
FDA Labeling Changes
There are currently no FDA labeling changes available for this drug.
Uses
- first aid to prevent bacteria contamination in minor cuts and scrapes
History
There is currently no drug history available for this drug.
Other Information
There are no additional details available for this product.
Sources
Benzethonium Chloride Plus Dyclonine Hydrochloride Manufacturers
- Cvs Pharmacy
Benzethonium Chloride Plus Dyclonine Hydrochloride | Cvs Pharmacy
Clean affected area apply a small amount on the area 1-3 times daily let dry a second coating may be applied for extra protection to remove, apply more Liquid Bandage and quickly wipe off finger nail polish remover may dissolve Liquid Bandage - Premier Value
Benzethonium Chloride Plus Dyclonine Hydrochloride | Blenheim Pharmacal, Inc.
The patient should be placed on a standard cholesterol-lowering diet before receiving lovastatin and should continue on this diet during treatment with lovastatin (see NCEP Treatment Guidelines for details on dietary therapy). Lovastatin should be given with meals.
Adult Patients: The usual recommended starting dose is 20 mg once a day given with the evening meal. The recommended dosing range is 10-80 mg/day in single or two divided doses; the maximum recommended dose is 80 mg/day. Doses should be individualized according to the recommended goal of therapy (see NCEP Guidelines and CLINICAL PHARMACOLOGY). Patients requiring reductions in LDL-C of 20% or more to achieve their goal (see INDICATIONS AND USAGE) should be started on 20 mg/day of lovastatin. A starting dose of 10 mg may be considered for patients requiring smaller reductions. Adjustments should be made at intervals of 4 weeks or more.
Cholesterol levels should be monitored periodically and consideration should be given to reducing the dosage of lovastatin if cholesterol levels fall significantly below the targeted range.
Dosage In Patients Taking Cyclosporine Or Danazol:In patients taking cyclosporine or danazol concomitantly with lovastatin (see WARNINGS, Myopathy/Rhabdomyolysis), therapy should begin with 10 mg of lovastatin and should not exceed 20 mg/day.
Dosage In Patients Taking Amiodarone Or Verapamil:In patients taking amiodarone or verapamil concomitantly with lovastatin, the dose should not exceed 40 mg/day (see WARNINGS, Myopathy/Rhabdomyolysis and PRECAUTIONS, Drug Interactions, Other Drug Interactions).
Adolescent Patients (10-17 Years Of Age) With Heterozygous Familial Hypercholesterolemia:The recommended dosing range is 10-40 mg/day; the maximum recommended dose is 40 mg/day. Doses should be individualized according to the recommended goal of therapy (see NCEP Pediatric Panel Guidelines††, CLINICAL PHARMACOLOGY, and INDICATIONS AND USAGE). Patients requiring reductions in LDL-C of 20% or more to achieve their goal should be started on 20 mg/day of lovastatin. A starting dose of 10 mg may be considered for patients requiring smaller reductions. Adjustments should be made at intervals of 4 weeks or more.
Concomitant Lipid-Lowering Therapy:Lovastatin is effective alone or when used concomitantly with bile-acid sequestrants. If lovastatin is used in combination with gemfibrozil, other fibrates or lipid-lowering doses (≥ 1g/day) of niacin, the dose of lovastatin should not exceed 20 mg/day (see WARNINGS, Myopathy/Rhabdomyolysis and PRECAUTIONS, Drug Interactions).
Dosage In Patients With Renal Insufficiency:In patients with severe renal insufficiency (creatinine clearance <30 mL/min), dosage increases above 20 mg/day should be carefully considered and, if deemed necessary, implemented cautiously (see CLINICAL PHARMACOLOGY and WARNINGS, Myopathy/Rhabdomyolysis).
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†† National Cholesterol Education Program (NCEP): Highlights of the Report of the Expert Panel on Blood Cholesterol Levels in Children and Adolescents. Pediatrics. 89(3):495-501. 1992.
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