Medidex is not a provider of medical services and all information is provided for the convenience of the user. No medical decisions should be made based on the information provided on this website without first consulting a licensed healthcare provider.This website is intended for persons 18 years or older. No person under 18 should consult this website without the permission of a parent or guardian.
ZINC OXIDE, MENTHOL, UNSPECIFIED FORM, and TRETINOIN
×
Overview
What is DERMAWERX ZMT PAK?
Tretinoin Gel, USP and Tretinoin Cream, USP are used for the topical treatment of acne vulgaris. Each gram of tretinoin gel contains tretinoin in either of two strengths, 0.025% (0.25 mg) or 0.01% (0.1 mg) in a gel vehicle of hydroxypropyl cellulose, butylated hydroxytoluene, and alcohol (denatured with
-butyl alcohol and brucine sulfate) 90% w/w. Each gram of tretinoin cream contains tretinoin in either of three strengths, 0.1% (1 mg), 0.05% (0.5 mg), or 0.025% (0.25 mg) in a hydrophilic cream vehicle of: stearic acid, isopropyl myristate, polyoxyl 40 stearate, stearyl alcohol, xanthan gum, sorbic acid, butylated hydroxytoluene, and purified water. Chemically, tretinoin is
-retinoic acid. It has a molecular weight of 300.44 and has the following structural formula:
What does DERMAWERX ZMT PAK look like?
What are the available doses of DERMAWERX ZMT PAK?
Sorry No records found.
What should I talk to my health care provider before I take DERMAWERX ZMT PAK?
Sorry No records found
How should I use DERMAWERX ZMT PAK?
A moisture barrier that prevents and helps heal skin irritation from: urine, diarrhea, perspiration, fistula damage, feeding tube site leakage, wound drainage (peri-wound skin), minor burns, cuts, scrapes, itching
Cleanse skin gently with mild skin cleanser. Pat dry or allow to air dry. Apply a thin layer of Calmoseptine Ointment to reddened or irritated skin 2-4 times daily, or after each incontinent episode or diaper change to promote comfort and long lasting protection.
What interacts with DERMAWERX ZMT PAK?
Sorry No Records found
What are the warnings of DERMAWERX ZMT PAK?
Sorry No Records found
What are the precautions of DERMAWERX ZMT PAK?
Sorry No Records found
What are the side effects of DERMAWERX ZMT PAK?
Sorry No records found
What should I look out for while using DERMAWERX ZMT PAK?
Use of the product should be discontinued if hypersensitivity to any of the ingredients is noted.
For external use only.
In case of accidental ingestion contact a physician or poison control center immediately. If condition worsens or does not improve within 7 days, consult a doctor.
What might happen if I take too much DERMAWERX ZMT PAK?
If medication is applied excessively, no more rapid or better results will be obtained and marked redness, peeling, or discomfort may occur. Oral ingestion of the drug may lead to the same side effects as those associated with excessive oral intake of Vitamin A.
How should I store and handle DERMAWERX ZMT PAK?
Store the generator at 20-25°C (68-77°F) [See
USP].How Supplied Alendronate sodium tablets, USP, 70 mg - white to off-white oval tablet embossed with “" on one side and “” on the other side. They are supplied as follows:NDC # 63187-580-04 Unit-of-use Blister Package of 4
Storage Alendronate Sodium Tablets: How Supplied Alendronate sodium tablets, USP, 70 mg - white to off-white oval tablet embossed with “" on one side and “” on the other side. They are supplied as follows:NDC # 63187-580-04 Unit-of-use Blister Package of 4
Storage Alendronate Sodium Tablets: How Supplied Alendronate sodium tablets, USP, 70 mg - white to off-white oval tablet embossed with “" on one side and “” on the other side. They are supplied as follows:NDC # 63187-580-04 Unit-of-use Blister Package of 4
Storage Alendronate Sodium Tablets: How Supplied Alendronate sodium tablets, USP, 70 mg - white to off-white oval tablet embossed with “" on one side and “” on the other side. They are supplied as follows:NDC # 63187-580-04 Unit-of-use Blister Package of 4
Storage Alendronate Sodium Tablets: How Supplied Alendronate sodium tablets, USP, 70 mg - white to off-white oval tablet embossed with “" on one side and “” on the other side. They are supplied as follows:NDC # 63187-580-04 Unit-of-use Blister Package of 4
Storage Alendronate Sodium Tablets:
×
Clinical Information
Chemical Structure
No Image found
Clinical Pharmacology
Although the exact mode of action of tretinoin is unknown, current evidence suggests that topical tretinoin decreases cohesiveness of follicular epithelial cells with decreased microcomedo formation. Additionally, tretinoin stimulates mitotic activity and increased turnover of follicular epithelial cells causing extrusion of the comedones.
Non-Clinical Toxicology
Use of the product should be discontinued if hypersensitivity to any of the ingredients is noted.
For external use only.
In case of accidental ingestion contact a physician or poison control center immediately. If condition worsens or does not improve within 7 days, consult a doctor.
Concomitant topical medication, medicated or abrasive soaps and cleansers, soaps and cosmetics that have a strong drying effect, and products with high concentrations of alcohol, astringents, spices or lime should be used with caution because of possible interaction with tretinoin. Particular caution should be exercised in using preparations containing sulfur, resorcinol, or salicylic acid with tretinoin. It also is advisable to "rest" a patient's skin until the effects of such preparations subside before use of tretinoin is begun.
If a reaction suggesting sensitivity or chemical irritation occurs, use of the medication should be discontinued. Exposure to sunlight, including sunlamps, should be minimized during the use of tretinoin, and patients with sunburn should be advised not to use the product until fully recovered because of heightened susceptibility to sunlight as a result of the use of tretinoin. Patients who may be required to have considerable sun exposure due to occupation and those with inherent sensitivity to the sun should exercise particular caution. Use of sunscreen products and protective clothing over treated areas is recommended when exposure cannot be avoided. Weather extremes, such as wind or cold, also may be irritating to patients under treatment with tretinoin.
Tretinoin preparations for acne treatment should be kept away from the eyes, the mouth, angles of the nose, and mucous membranes. Topical use may induce severe local erythema and peeling at the site of application. If the degree of local irritation warrants, patients should be directed to use the medication less frequently, discontinue use temporarily, or discontinue use altogether. Tretinoin has been reported to cause severe irritation on eczematous skin and should be used with utmost caution in patients with this condition.
The skin of certain sensitive individuals may become excessively red, edematous, blistered, or crusted. If these effects occur, the medication should either be discontinued until the integrity of the skin is restored, or the medication should be adjusted to a level the patient can tolerate. True contact allergy to topical tretinoin is rarely encountered. Temporary hyper- or hypopigmentation has been reported with repeated application of a tretinoin preparation. Some individuals have been reported to have heightened susceptibility to sunlight while under treatment with tretinoin. To date, all adverse effects of tretinoin have been reversible upon discontinuance of therapy
×
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.
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. 315.72
×
Tips
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).
