INLIFAY ANTIFUNGAL- miconazole nitrate 2% antifungal cream

Inlifay ANTIFUNGAL by

Drug Labeling and Warnings

Inlifay ANTIFUNGAL by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Miconazole Nitrate 2% w/w

Purpose

Antifungal

Use

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

Warnings

For external use only.

Do not use

you are allergic to miconazole or any of the ingredients in this product

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.

Stop Use

Irritation occurs Condition persists for more than 2 weeks or worsens

Ask Doctor

Irritation occurs Condition persists for more than 2 weeks or worsens

Keep Oot Of Reach Of Children

If swallowed,get medical help or contact a Poison Control Center right away.

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.

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 ingredients

Aloe, Borneol, Cnidium, Dictamnus, Euphorbia, Glycerin, Light liquid paraffin, Medical petrolatum, Natural menthol, Purified water, Sophora Flavescens, Stearic acid, Stemona, Triethanolamine, Vitamin E

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

INLIFAY ANTIFUNGAL 
miconazole nitrate 2% antifungal cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-252
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M)	MICONAZOLE NITRATE	2 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
LEVOMENTHOL (UNII: BZ1R15MTK7)
WATER (UNII: 059QF0KO0R)
STEMONA TUBEROSA ROOT (UNII: 7S9328671Z)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
ORIGANUM DICTAMNUS FLOWERING TOP (UNII: 9RBR98LSD9)
BORNEOL (UNII: M89NIB437X)
STEARIC ACID (UNII: 4ELV7Z65AP)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
EUPHORBIA HIRTA (UNII: L13YF113GN)
WHITE PETROLATUM (UNII: B6E5W8RQJ4)
CNIDIUM SEED (UNII: V1IA3S3CUS)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
ALOE (UNII: V5VD430YW9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-252-01	100 g in 1 BOTTLE; Type 0: Not a Combination Product	01/22/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	01/22/2026

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-252)