Active Ingredient
Miconazole nitrate, USP 2% (100 mg in each applicator)
The following Structured Product Label (SPL) was submitted to the FDA by Quality Choice (chain Drug Marketing Association) for the product Miconazole 7 (NDC 63868-198). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, when using this product, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Miconazole nitrate, USP 2% (100 mg in each applicator)
Vaginal antifungal
For vaginal use only
if you have never had a vaginal yeast infection diagnosed by a doctor
taking the prescription blood thinning medicine warfarin, because bleeding or bruising may occur
ask a health professional before use.
If swallowed, get medical help or contact a Poison Control Center right away.
benzoic acid, butylated hydroxyanisole, mineral oil, oleoyl polyoxylglycerides, pegoxol 7 stearate, purified water
1-800-432-8534 between 9 am and 4 pm EST, Monday–Friday.
QC® QUALITY CHOICE
NDC 63868-198-45
*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
1.59 OZ NET WT (45 g) Tube
7 Day Vaginal Cream (1 Tube) with 1 Reusable Applicator
* Please review the disclaimer below.