Label: MICONAZOLE 7- miconazole nitrate cream
- NDC Code(s): 68788-8661-4
- Packager: Preferred Pharmaceuticals Inc.
- This is a repackaged label.
- Source NDC Code(s): 0904-7734
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 13, 2024
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Drug Facts
- Active ingredient
- Purpose
- Uses
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Warnings
For vaginal use only
Ask a doctor before use if you have
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- vaginal itching and discomfort for the first time
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- lower abdominal, back, or shoulder pain, fever, chills, nausea, vomiting, or foul-smelling vaginal discharge. You may have a more serious condition.
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- 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.
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- 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
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- 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).
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- do not have vaginal intercourse
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- mild increase in vaginal burning, itching or irritation may occur
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- if you do not get complete relief ask a doctor before using another product.
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Directions
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- before using this product read the enclosed consumer information leaflet for complete directions and information
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adults and children 12 years of age and over:
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- applicator:insert 1 applicatorful into the vagina at bedtime for 7 nights in a row. Wash applicator after use.
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- use the same tube of cream if you have itching and irritation on the skin outside the vagina. Squeeze a small amount of cream onto your fingertip. Apply to itchy, irritated skin outside the vagina (vulva). Use 2 times daily for up to 7 days as needed.
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- children under 12 years of age: ask a doctor
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Other information
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- to open tube: unscrew cap, lift tab, and pull to remove foil seal prior to use
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- do not use if foil seal on tube opening is broken or missing
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- do not purchase if carton is open
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- store at room temperature 20°to 25°C (68°to 77°F)
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- before using any medication, read all label direction. Keep carton, it contains important information.
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- Relabeled By: Preferred Pharmaceuticals Inc.
- Inactive ingredients
- Questions?
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Principal display panel
Compare to the active ingredient in Monistat® 7 Vaginal Cream*
Miconazole 7
Miconazole Nitrate Vaginal Cream, USP 2%
(Miconazole Nitrate 100 mg per applicator)
2%
Vaginal Antifungal
Cures most vaginal yeast infections
Relieves associated external itching and irritation
7 day vaginal cream (1 tube) with 1 reusable applicator
NET WT OZ (g) Tube
*This product is not affiliated with, manufactured by, or produced by the makers or owners of Monistat®.
Distributed by:
MAJOR® PHARMACEUTICALS
Indianapolis, IN 46268
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INGREDIENTS AND APPEARANCE
MICONAZOLE 7
miconazole nitrate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68788-8661(NDC:0904-7734) Route of Administration VAGINAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 20 mg in 1 g Inactive Ingredients Ingredient Name Strength 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) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68788-8661-4 1 in 1 CARTON 05/13/2024 1 45 g in 1 TUBE, WITH APPLICATOR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA074164 04/21/2009 Labeler - Preferred Pharmaceuticals Inc. (791119022) Registrant - Preferred Pharmaceuticals Inc. (791119022) Establishment Name Address ID/FEI Business Operations Preferred Pharmaceuticals Inc. 791119022 RELABEL(68788-8661)
