Label: NYSTATIN powder

  • NDC Code(s): 69315-306-15, 69315-306-30, 69315-306-60
  • Packager: Leading Pharma, LLC
  • Category: HUMAN PRESCRIPTION DRUG LABEL

Drug Label Information

Updated April 18, 2024

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  • DESCRIPTION

    Nystatin is a polyene antifungal antibiotic obtained from Streptomyces noursei. The molecular formula for Nystatin is C47H75NO17. The molecular weight of Nystatin is 926.1.
    Structural formula:

    Chemical-structure

    Nystatin topical powder is for dermatologic use.
    Nystatin topical powder contains 100,000 nystatin units per gram dispersed in talc.

  • CLINCAL 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

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

    Nystatin topical powder is not indicated for systemic, oral, intravaginal or ophthalmic use.

  • CONTRAINDICATIONS

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

  • PRECAUTIONS

    General

    Nystatin topical powder 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

  • HOW SUPPLIED

    Nystatin topical powder is supplied as 100,000 units nystatin per gram in plastic squeeze bottles:


    15g (NDC 69315-306-15)

    30g (NDC 69315-306-30)

    60g (NDC 69315-306-60)

    STORAGE

    Store at 20°C to 25°C (68°F to 77°F)[see USP Controlled Room Temperature]; avoid excessive heat (40°C/104°F).

    Keep tightly closed.

    Manufactured for:

    Leading Pharma LLC, Fairfield, NJ 07004

    Manufactured by:

    Lyne Laboratories, Inc. Brockton, MA 02301


    R1-01/20

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Container-100000unit15gmContainer-100000unit30gmContainer-100000unit60gm

  • INGREDIENTS AND APPEARANCE
    NYSTATIN 
    nystatin powder
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:69315-306
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NYSTATIN (UNII: BDF1O1C72E) (NYSTATIN - UNII:BDF1O1C72E) NYSTATIN100000 [USP'U]  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    TALC (UNII: 7SEV7J4R1U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69315-306-1515 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/23/2018
    2NDC:69315-306-3030 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/23/2018
    3NDC:69315-306-6060 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/23/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA20883804/23/2018
    Labeler - Leading Pharma, LLC (079575060)
    Registrant - Lyne Laboratories, Inc (053510459)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lyne Laboratories, Inc053510459manufacture(69315-306)