Anti-fungal Powder Miconazole Nitrate Powder
NDC Package 79481-0621-1

The code 79481-0621-1 identifies a specific commercial package of 71 g in 1 bottle, plastic of Anti-fungal Powder Miconazole Nitrate, a human over the counter drug labeled by Meijer Distribution Inc. This powder is formulated for topical use and contains miconazole nitrate as the active substance.

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Meijer Distribution Inc on August 28, 2023. The current certification is valid through December 31, 2026.

This medication is used to treat vaginal yeast infections. Miconazole reduces vaginal burning, itching, and discharge that may occur with this condition. This medication is an azole antifungal. It works by stopping the growth of yeast (fungus) that causes the infection. The vaginal product comes in 2 forms (a vaginal cream or tablet). Some products also come with a skin cream to be applied to the area around the outside of the vagina. Ask your doctor before using this medication for self-treatment if this is your first vaginal infection. This medication only works for vaginal fungal infections. You may have a different type of infection (such as bacterial vaginosis) and may need a different medication. If you have fever, chills, flu-like symptoms, stomach/abdominal pain, or a bad-smelling vaginal discharge, do not use this medication. Contact your doctor right away because these may be signs of a more serious infection.

For medical billing and reimbursement, this package follows the 11-digit CMS format: 79481062101. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.