MICONAZOLE NITRATE cream

Miconazole Nitrate by

Drug Labeling and Warnings

Miconazole Nitrate by is a Otc medication manufactured, distributed, or labeled by Taro Pharmaceuticals U.S.A., Inc., Taro Pharmaceuticals Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Can I use Miconazole Nitrate Vaginal Cream USP (4%) during my menstrual period?

Yes, this product can be used during your menstrual period. In fact, many women get vaginal yeast infections just before their period because of hormonal changes. Using miconazole nitrate vaginal cream during your period will not affect how well this product works. If you have started treatment and your period occurs, you should complete the full course of treatment.

Do not use tampons while using this product, because tampons may remove some of the drug from the vagina. Use deodorant-free sanitary napkins or pads instead, and change them often.

Can I use other vaginal products with Miconazole Nitrate Vaginal Cream USP (4%)?

This drug should not be used with other vaginal products.

How can I get the best results when treating my infection?

What warnings should I know about when using Miconazole Nitrate Vaginal Cream USP (4%)?

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:

Ask a doctor or pharmacist before use if you are taking the prescription blood thinning medicine, warfarin (coumadin), because bleeding or bruising may occur.

When using this product:

Stop use and ask your doctor if:

If pregnant or breastfeeding, 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.

What side effects may occur with Miconazole Nitrate Vaginal Cream USP (4%)?

A mild increase in vaginal burning, itching, or irritation may occur when the applicator containing the cream is inserted. Abdominal cramping has also been reported.

Stop using miconazole nitrate vaginal cream USP (4%) and consult your doctor if you have abdominal pain, hives, skin rash, or if you have severe vaginal burning, itching, or irritation or swelling.

What should I do if I have questions about Miconazole Nitrate Vaginal Cream USP (4%)?

Questions of a medical nature should be taken up with your doctor. If you have any other questions or need more information on this product, call 1-866-923-4914.

Other information:

Active ingredient: miconazole nitrate USP 4%.

Inactive ingredients: cetyl alcohol, isopropyl myristate, polysorbate 60, polysorbate 80, potassium hydroxide, propylene glycol, purified water, sorbitan monostearate, stearyl alcohol.

How should I use Miconazole Nitrate Vaginal Cream USP (4%) with 3 disposable applicators?

This product is for adults and children 12 years of age and over. For children under 12 years, ask a doctor.

Directions for using the vaginal cream:

Begin treatment before going to bed:

1. To open the tube, unscrew the cap. The first time the tube is opened, press the sharp point of the cap into the sealed end of the tube. Push down firmly until the seal is broken. (See pictures.)
Figure
2. Attach the applicator to the tube of cream by placing "A" end of the applicator firmly onto tube of cream.
Figure
3. Gently squeeze the cream into the applicator, continue squeezing until applicator is full. Separate the applicator from the tube. DO NOT release pressure on the tube until you have separated it from the filled applicator. After each use, replace the cap and roll up the tube from the bottom.
4. Hold the barrel as shown in the picture.
Figure
5. Gently insert the applicator into the vagina as far as it will go comfortably. This can be done while lying on your back with your knees bent (as shown in the picture) or while standing with your feet apart and your knees bent.
Figure
6. With one hand holding the barrel, use the other hand to push the plunger all the way in to place the cream as far back in the vagina as possible. Then remove both parts of the applicator from the vagina.
7. Throw away applicator after use. Do not flush in toilet..
8. Lie down as soon as possible after inserting the cream. This will reduce leakage.
9. Repeat steps 2 through 8 before going to bed for the next 2 days. You may want to use deodorant-free pads or pantyshields to protect your clothing during the time that you are using miconazole nitrate vaginal cream USP (4%). This is because the cream can leak or you may get some discharge. Do not use tampons, douches, spermicides, condoms, or diaphragms until after you have completed treatment and your symptoms are gone.

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

LPK-5199-3
0220-3
35

  • PRINCIPAL DISPLAY PANEL - 25 g Tube Carton

    CURES most vaginal
    YEAST INFECTIONS

    NDC: 51672-2070-9

    3 Day Treatment

    Miconazole 3
    Miconazole Nitrate Vaginal Cream USP (4%)
    Vaginal Antifungal

    One 0.9 oz (25 g) tube of 3 Day Vaginal Cream with
    3 Disposable Applicators

    PRINCIPAL DISPLAY PANEL - 25 g Tube Carton
  • INGREDIENTS AND APPEARANCE
    MICONAZOLE NITRATE 
    miconazole nitrate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 51672-2070
    Route of AdministrationVAGINAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Miconazole Nitrate (UNII: VW4H1CYW1K) (Miconazole - UNII:7NNO0D7S5M) Miconazole Nitrate40 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    cetyl alcohol (UNII: 936JST6JCN)  
    isopropyl myristate (UNII: 0RE8K4LNJS)  
    polysorbate 60 (UNII: CAL22UVI4M)  
    polysorbate 80 (UNII: 6OZP39ZG8H)  
    potassium hydroxide (UNII: WZH3C48M4T)  
    propylene glycol (UNII: 6DC9Q167V3)  
    water (UNII: 059QF0KO0R)  
    sorbitan monostearate (UNII: NVZ4I0H58X)  
    stearyl alcohol (UNII: 2KR89I4H1Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 51672-2070-91 in 1 CARTON03/02/2005
    125 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANDAANDA07677303/02/2005
    Labeler - Taro Pharmaceuticals U.S.A., Inc. (145186370)
    Establishment
    NameAddressID/FEIBusiness Operations
    Taro Pharmaceuticals Inc.206263295MANUFACTURE(51672-2070)

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