Thursday, 8 March 2012

Nystatin Cream




Dosage Form: cream
Nystatin

Cream USP, 100,000 units per gram

Rx only


FOR TOPICAL USE ONLY • NOT FOR OPHTHALMIC USE



Nystatin Cream Description


Nystatin is a polyene antifungal antibiotic obtained from Streptomyces nursei.


Structural formula:


C47H75NO17         Molecular Weight: 926.13



Nystatin Cream is for dermatologic use.


Nystatin Cream for topical use, contains 100,000 USP nystatin units per gram in an aqueous, perfumed cream base containing aluminum hydroxide gel, ceteareth-15, glyceryl monostearate, polyethylene glycol 400 monostearate, propylene glycol, purified water, simethicone emulsion, sorbitol solution, titanium dioxide, white petrolatum, with methylparaben and propylparaben as preservatives and, if necessary, sodium hydroxide for pH adjustment.



Nystatin Cream - Clinical Pharmacology



Pharmacokinetics


Nystatin is not absorbed from intact skin or mucous membrane.



Microbiology


Nystatin is an antibiotic which is both fungistatic and fungicidal in vitro against a wide variety of yeasts and yeast-like fungi, including Candida albicans, C. parapsilosis, C. tropicalis, C. guilliermondi, C. pseudotropicalis, C. krusei, Torulopsis glabrata, Tricophyton rubrum, T. mentagrophytes. Nystatin acts by binding to sterols in the cell membrane of susceptible species resulting in a change in membrane permeability and the subsequent leakage of intracellular components. On repeated subculturing with increasing levels of nystatin, Candida albicans does not develop resistance to nystatin. Generally, resistance to nystatin does not develop during therapy. However, other species of Candida (C. tropicalis, C. guilliermondi, C. krusei, and C. stellatoides) become quite resistant on treatment with nystatin and simultaneously become cross resistant to amphotericin as well. This resistance is lost when the antibiotic is removed. Nystatin exhibits no appreciable activity against bacteria, protozoa, or viruses.



Indications and Usage for Nystatin Cream


Nystatin Cream is indicated in the treatment of cutaneous or mucocutaneous mycotic infections caused by Candida albicans and other susceptible Candida species.


This cream is not indicated for systemic, oral, intravaginal or ophthalmic use.



Contraindications


Nystatin Cream is contraindicated in patients with a history of hypersensitivity to any of its components.



Precautions



General


Nystatin Cream should not be used for the treatment of systemic, oral, intravaginal or ophthalmic infections.


If irritation or sensitization develops, treatment should be discontinued and appropriate measures taken as indicated. It is recommended that KOH smears, cultures, or other diagnostic methods be used to confirm the diagnosis of cutaneous or mucocutaneous candidiasis and to rule out infection caused by other pathogens.



INFORMATION FOR THE PATIENT


Patients using this medication should receive the following information and instructions:


  1. The patient should be instructed to use this medication as directed (including the replacement of missed doses). This medication is not for any disorder other than that for which it is prescribed.

  2. Even if symptomatic relief occurs within the first few days of treatment, the patient should be advised not to interrupt or discontinue therapy until the prescribed course of treatment is completed.

  3. If symptoms of irritation develop, the patient should be advised to notify the physician promptly.


Laboratory Tests


If there is a lack of therapeutic response, KOH smears, cultures, or other diagnostic methods should be repeated.



Carcinogenesis, Mutagenesis, Impairment of Fertility


No long-term animal studies have been performed to evaluate the carcinogenic potential of nystatin. No studies have been performed to determine the mutagenicity of nystatin or the effects on male or female fertility.



Pregnancy


Teratogenic Effects

Category C


Animal reproduction studies have not been conducted with any Nystatin Cream. It also is not known whether this cream can cause fetal harm when used by a pregnant woman or can affect reproductive capacity. Nystatin Cream should be prescribed for a pregnant woman only if the potential benefit to the mother outweighs the potential risk to the fetus.



Nursing Mothers


It is not known whether nystatin is excreted in human milk. Caution should be exercised when nystatin is prescribed for a nursing woman.



Pediatric Use


Safety and effectiveness have been established in the pediatric population from birth to 16 years.


(See DOSAGE AND ADMINISTRATION.)



Geriatric Use


Clinical studies with Nystatin Cream did not include sufficient numbers of subjects aged 65 years and older to determine whether they respond differently than younger subjects. Other reported clinical experience has not identified differences in responses between elderly and younger patients, but greater sensitivity of some older individuals cannot be ruled out.



Adverse Reactions


The frequency of adverse events reported in patients using Nystatin Cream is less than 0.1%. The more common events that were reported include allergic reactions, burning, itching, rash, eczema, and pain on application.


(See PRECAUTIONS: General.)



Nystatin Cream Dosage and Administration



Adults and Pediatric Patients (Neonates and Older)


Apply liberally to affected areas twice daily or as indicated until healing is complete.



How is Nystatin Cream Supplied


Nystatin Cream USP is a smooth yellow to light green cream with a characteristic perfume odor.


Nystatin Cream USP is supplied in 15 g (NDC 51672-1289-1) and 30 g (NDC 51672-1289-2) tubes providing 100,000 USP Nystatin Units per gram.



Store at 20° to 25°C (68° to 77°F) [see USP Controlled Room Temperature]. Avoid freezing.



Mfd. by: Taro Pharmaceuticals Inc., Brampton, Ontario, Canada L6T 1C1


Dist. by: Taro Pharmaceuticals U.S.A., Inc., Hawthorne, NY 10532


Revised: August, 2010


PK-1161-4

107



PRINCIPAL DISPLAY PANEL - 30 g Tube Carton


NDC 51672-1289-2


30 g


Nystatin

Cream USP, 100,000 units per gram


FOR EXTERNAL USE ONLY.

NOT FOR OPHTHALMIC USE.


Rx only


Keep this and all medications out of the reach of children.


TARO










NYSTATIN 
nystatin  cream










Product Information
Product TypeHUMAN PRESCRIPTION DRUGNDC Product Code (Source)51672-1289
Route of AdministrationTOPICALDEA Schedule    








Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Nystatin (Nystatin)Nystatin100000 [USP'U]  in 1 g


























Inactive Ingredients
Ingredient NameStrength
petrolatum 
glyceryl monostearate 
ceteareth-15 
water 
propylene glycol 
methylparaben 
propylparaben 
titanium dioxide 
algeldrate 
sorbitol 
sodium hydroxide 


















Product Characteristics
ColorYELLOW (smooth yellow to light green)Score    
ShapeSize
FlavorImprint Code
Contains      






















Packaging
#NDCPackage DescriptionMultilevel Packaging
151672-1289-11 TUBE In 1 CARTONcontains a TUBE
115 g In 1 TUBEThis package is contained within the CARTON (51672-1289-1)
251672-1289-21 TUBE In 1 CARTONcontains a TUBE
230 g In 1 TUBEThis package is contained within the CARTON (51672-1289-2)










Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA06402201/28/1993


Labeler - Taro Pharmaceuticals U.S.A., Inc. (145186370)









Establishment
NameAddressID/FEIOperations
Taro Pharmaceuticals Inc.206263295MANUFACTURE
Revised: 08/2011Taro Pharmaceuticals U.S.A., Inc.

More Nystatin Cream resources


  • Nystatin Cream Use in Pregnancy & Breastfeeding
  • Nystatin Cream Support Group
  • 6 Reviews for Nystatin - Add your own review/rating


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