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Menthol and Lidocaine
Overview
What is Provenza?
Provenza is a topically administered patch that combines an external analgesic and a topical anesthetic.
Each patch contains:
Menthol 1%
Lidocaine 4%
Each patch contains the following inactive ingredients: Silicon Dioxide
What does Provenza look like?
What are the available doses of Provenza?
Sorry No records found.
What should I talk to my health care provider before I take Provenza?
Sorry No records found
How should I use Provenza?
Provenza is indicated for relief of pain associated with arthritis, simple backaches, bursitis, tendonitis, muscle strains, sprains, bruises, cramps.
Clean and dry affected area, cut open pouch and remove patch, remove protective film and apply directly to area of pain, apply to affected area not more than 3 times daily, wash hands with soap after applying patch, reseal pouch containing unused patches. Use only one patch at a time, and maximum of three patches / day. Children under 12 should consult physician prior to use.
What interacts with Provenza?
Sorry No Records found
What are the warnings of Provenza?
Sorry No Records found
What are the precautions of Provenza?
Sorry No Records found
What are the side effects of Provenza?
Sorry No records found
What should I look out for while using Provenza?
What might happen if I take too much Provenza?
Sorry No Records found
How should I store and handle Provenza?
Provenza patch is supplied in 8cm x 10cm packed in boxes of 15 and 30.15ct Box, NDC 69336-600-1530ct Box, NDC 69336-600-30Provenza patch is supplied in 8cm x 10cm packed in boxes of 15 and 30.15ct Box, NDC 69336-600-1530ct Box, NDC 69336-600-30Provenza patch is supplied in 8cm x 10cm packed in boxes of 15 and 30.15ct Box, NDC 69336-600-1530ct Box, NDC 69336-600-30
Clinical Information
Chemical Structure
No Image foundClinical Pharmacology
Non-Clinical Toxicology
Caution must be exercised in the administration of 3% and 5% Sodium Chloride Injection, USP to patients treated with drugs that may increase the risk of sodium and fluid retention, such as corticosteroids.Caution is advised in patients treated with lithium. Renal sodium and lithium clearance may be increased during the administration of 3% and 5% Sodium Chloride Injection, USP. Administration of 3% and 5% Sodium Chloride Injection, USP may, therefore, result in decreased lithium levels.
For external use only.
Use only as directed.
Do not bandage tightly or use with a heating pad.
Avoid contact with eyes and mucous membranes.
Do not apply to wound or damaged, broken or irritated skin.
Stop use and ask doctor if condition worsens, redness is present, irritation develops, symptoms persist for more than 7 days or clear up and occur again within a few days.
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
A total of 440 drugs (1549 brand and generic names) are known to interact with Imbruvica (ibrutinib). 228 major drug interactions (854 brand and generic names) 210 moderate drug interactions (691 brand and generic names) 2 minor drug interactions (4 brand and generic names) Show all medications in the database that may interact with Imbruvica (ibrutinib).