![MICONAZOLE 7 (MICONAZOLE NITRATE) CREAM [CHAIN DRUG CONSORTIUM, LLC]](https://medic.hrt.org//dailymed/images/74369ba9-2021-467e-bf1d-c4e7284535da/miconazole-7-cream-1.jpg)
| NDC | 68016-073-01 |
| Set ID | 74369ba9-2021-467e-bf1d-c4e7284535da |
| Category | HUMAN OTC DRUG LABEL |
| Packager | Chain Drug Consortium, LLC |
| Generic Name | |
| Product Class | Azole Antifungal |
| Product Number | |
| Application Number | ANDA074164 |
- Drug Facts
- Active ingredient
- Purpose
- Uses
-
Warnings
For vaginal use only
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
- if you do not get complete relief ask a doctor before using another product.
-
Directions
- 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:
- applicator: insert 1 applicatorful into the vagina at bedtime for 7 nights in a row. Wash applicator after use.
- 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.
- children under 12 years of age: ask a doctor
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Other information
- to open tube: unscrew cap, lift tab, and pull to remove foil seal prior to use
- do not use if foil seal on tube opening is broken or missing
- do not purchase if carton is open
- store at room temperature 20°-25°C (68°-77°F) [see USP Controlled Room Temperature] excursions permitted to 15°-30°C (59°-86°F).
- before using any medication, read all label directions. Keep carton, it contains important information.
- Inactive ingredients
- Questions?
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Principal display label
COMPARE TO THE ACTIVE INGREDIENT IN MONISTAT® 7 VAGINAL CREAM*
Miconazole 7
Miconazole Nitrate Vaginal Cream USP, 2%
Vaginal Antifungal
(Miconazole Nitrate 100 mg per applicator)
Cures most vaginal yeast infections
and Relieves Associated External Itching and Irritation
7 Day Vaginal Cream (1 Tube)
with 1 reusable applicator
NET WT OZ (g)
*This product is not affiliated with, manufactured by, or produced by the makers or owners of Monistat®.
Distributed by:
Pharmacy Value Alliance, LLC
407 East Lancaster Avenue,
Wayne, PA 19087
- Package label
-
INGREDIENTS AND APPEARANCE
MICONAZOLE 7
miconazole nitrate creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68016-073 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:68016-073-01 1 in 1 CARTON 09/11/2003 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 09/11/2003 Labeler - Chain Drug Consortium, LLC (101668460)
