Label: MICONAZOLE 3 COMBINATION PACK- miconazole nitrate kit

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Drug Application

Drug Label Information

Updated June 21, 2022

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  • Drug Facts

  • Active ingredients

    Miconazole nitrate, USP 200 mg (in each suppository)
    Miconazole nitrate, USP 2% (external cream)

  • Purpose

    Vaginal antifungal

    Vaginal antifungal

  • Uses

    • treats vaginal yeast infections
    • relieves external itching and irritation due to a vaginal yeast infection
  • Warnings

    For vaginal use only

    Do not use

    if you have never had a vaginal yeast infection diagnosed by a doctor

    Ask a doctor before use if you have

    • vaginal itching and discomfort for the first time
    • lower abdominal, back or shoulder pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge. You may have a more serious condition.
    • vaginal yeast infections often (such as once a month or 3 in 6 months). You could be pregnant or have a serious underlying medical cause for your symptoms, including diabetes or a weakened immune system.
    • been exposed to the human immunodeficiency virus (HIV) that causes AIDS

    Ask a doctor or pharmacist before use if you are

    taking the prescription blood thinning medicine warfarin, because bleeding or bruising may occur

    When using this product

    • do not use tampons, douches, spermicides or other vaginal products. Condoms and diaphragms may be damaged and fail to prevent pregnancy or sexually transmitted diseases (STDs).
    • do not have vaginal intercourse
    • mild increase in vaginal burning, itching or irritation may occur

    Stop use and ask a doctor if

    • symptoms do not get better in 3 days
    • symptoms last more than 7 days
    • you get a rash or hives, abdominal pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge

    If pregnant or breast-feeding,

    ask a health professional before use.

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • before using this product read the enclosed consumer information leaflet for complete directions and information
    • adults and children 12 years of age and over:
      • suppositories: insert 1 suppository into the vagina at bedtime for 3 nights in a row. Throw applicator away after use.
      • external cream: Use cap to puncture seal. Squeeze a small amount of cream onto your fingertip. Gently apply the cream onto the itchy, irritated skin outside the vagina. Use 2 times daily for up to 7 days, as needed.
    • children under 12 years of age: ask a doctor
  • Other information

    • do not use if suppository wrapper is missing or damaged (each suppository is individually wrapped)
    • do not use if seal over tube opening has been punctured or is not visible
    • do not purchase if carton is open
    • store at 20°-25°C (59°-86°F) [see USP Controlled Room Temperature] excursions permitted to 15º-30ºC (59º-86ºF)
  • Inactive ingredients

    • suppository: hydrogenated vegetable oil
    • external cream: benzoic acid, butylated hydroxyanisole, mineral oil, oleoyl polyoxylglycerides, pegoxol 7 stearate, purified water
  • Questions?

    Call 1-877-753-3935 Monday-Friday 9AM-5PM EST

  • Package display label

    Compare to the active ingredient in Monistat® 3††

    Miconazole 3

    MICONAZOLE NITRATE VAGINAL SUPPOSITORIES (200 mg)

    & MICONAZOLE NITRATE VAGINAL CREAM (2%)

    VAGINAL ANTIFUNGAL | COMBINATION PACK | 3-DAY TREATMENT

    • Cures most vaginal yeast infections
    • Relieves associated external itching & irritation

    3 VAGINAL SUPPOSITORIES WITH DISPOSABLE APPLICATORS PLUS EXTERNAL CREAM

    NET WT OZ (G) TUBE

    & SUPPOSITORIES 2.5 g EACH

    ††This product is not affiliated with, manufactured by, produced by the makers or owners of Monistat® 3.

    DISTRIBUTED BY: WALGREEN CO.

    200 WILMOT RD., DEERFIELD, IL 60015

  • Package label

    Miconazole nitrate, USP 200 mg (in each suppository), Miconazole nitrate, USP 2% (external cream)

    WALGREENS Vaginal Suppositories with Disposable Applicators plus External Cream

  • INGREDIENTS AND APPEARANCE
    MICONAZOLE 3 COMBINATION PACK 
    miconazole nitrate kit
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-9089
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-9089-031 in 1 PACKAGE, COMBINATION; Type 0: Not a Combination Product06/10/2022
    Quantity of Parts
    Part #Package QuantityTotal Product Quantity
    Part 11 BLISTER PACK 3 
    Part 21 TUBE 9 g
    Part 1 of 2
    MICONAZOLE 3 
    miconazole nitrate suppository
    Product Information
    Item Code (Source)NDC:0363-9093
    Route of AdministrationVAGINAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE200 mg
    Inactive Ingredients
    Ingredient NameStrength
    HYDROGENATED PALM KERNEL OIL (UNII: FM8D1RE2VP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    13 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07492606/10/2022
    Part 2 of 2
    MICONAZOLE 3 
    miconazole nitrate cream
    Product Information
    Item Code (Source)NDC:0363-9092
    Route of AdministrationVAGINAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE10 mg  in 0.5 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    APRICOT KERNEL OIL PEG-6 ESTERS (UNII: DRG3KJZ1TJ)  
    PEGOXOL 7 STEARATE (UNII: 3EW5AXE5X5)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    19 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07492606/10/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07492606/10/2022
    Labeler - Walgreens (008965063)
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