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Inlifay ANTIFUNGAL drug information

MICONAZOLE NITRATE 2% ANTIFUNGAL
Jiangxi Yudexi Pharmaceutical Co., LTD · TOPICAL

Product NDC: 85248-139

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameMICONAZOLE NITRATE 2% ANTIFUNGAL
Labeler / manufacturerJiangxi Yudexi Pharmaceutical Co., LTD
RouteTOPICAL
Drug classDrug class not supplied in source label
Product NDC85248-139
Label effective date2026-09-06

Official product label reference

Inlifay ANTIFUNGAL — Jiangxi Yudexi Pharmaceutical Co., LTD

This page contains 12 source sections for MICONAZOLE NITRATE 2% ANTIFUNGAL, topical route. Label set 4a832f39-ac11-d8b3-e063-6394a90acb39, version 2.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Use Helps relieve the itching, burning, cracking, and scaling associated with fungal infections such as athlete's foot,jock itch, and ringworm.

Purpose

Purpose Antifungal
Dosage and administration — label text
Directions Clean the affected area and dry thoroughly. Apply a thin layer to the affected area twice daily (morning and night). Supervise children in the use of this product. Use daily for the full treatment period as directed. This product is not effective on the scalp or nails.
Warnings
Warnings For external use only.
Active ingredient
Active Ingredient Miconazole Nitrate 2% w/w
Do not use
Do not use you are allergic to miconazole or any of the ingredients in this product
While using this medicine
When Using Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Do not use on children under 2 years of age unless directed by a doctor.
When to stop use and seek help
Stop Use Irritation occurs Condition persists for more than 2 weeks or worsens
Ask a doctor before use
Ask Doctor Irritation occurs Condition persists for more than 2 weeks or worsens
Child safety
Keep Oot Of Reach Of Children If swallowed,get medical help or contact a Poison Control Center right away.
Storage and handling
Other information 1. Keep in a cool and dry place, avoid direct sunlight. 2. Keep out of the reach of children to avoid accidental ingestion.
Inactive ingredient
Inactive ingredients Aloe, Borneol, Cnidium, Dictamnus, Euphorbia, Glycerin, Light liquid paraffin, Medical petrolatum, Natural menthol, Purified water, Sophora Flavescens, Stearic acid, Stemona, Triethanolamine, Vitamin E

Official sources and product identifiers

Substances listed: MICONAZOLE NITRATE

RxNorm identifiers: 998483

Package NDC codes

85248-139-01

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.