CHARMPOO ANTIFUNGAL CREAM- miconazole nitrate 2% antifungal cream cream

Charmpoo Antifungal Cream by

Drug Labeling and Warnings

Charmpoo Antifungal Cream by is a Otc medication manufactured, distributed, or labeled by Jiangxi Yudexi Pharmaceutical Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

miconazole nitrate 2% w/w

Purpose

Anti-fungal

Use

The product with Repair and Anti-ltch function effectively relieve skin discomfort, such as itching, athlete's foot eczema, jock itch, etc

Warnings

For external use only

Do not use

children under 2 years of age unless directed by a doctor.

When Using

avoid contact with the eyes.

Stop Use

·Irritation occurs ·There is no improvement within 4 weeks (for athlete's foot and fingworm) or within 2 weeks (for jock itch)

Ask Doctor

·Irritation occurs ·There is no improvement within 4 weeks (for athlete's foot and fingworm) or within 2 weeks (for jock itch)

Keep Oot Of Reach Of Children

lf swallowed, get medical help or contact a Poison controlcenter(1-800-222-1222)right away.

Directions

Apply suitable amount unto the affected skin 2-3 times daily and massage until absorbs.

Other information

·Do not use if seal on product opening is broken or missing ·Store at room temperature 15°-30°C(59°-86°F) ·Read all label directions. Keep carton, it contains important information.

Inactive ingredients

Purifed water, Aloe, Borneol, Chlorhexidine acetate, Cnidium, Dictamnus,Euphorbia, Glycerin, Lightliquid paraffn, Medical vaseline, Natural menthol Sophora Flavescens, Stearic acid, Stemona,Triethanolamine, Vitamin E

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CHARMPOO ANTIFUNGAL CREAM 
miconazole nitrate 2% antifungal cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-142
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
WATER (UNII: 059QF0KO0R)
MENTHOL (UNII: L7T10EIP3A)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
LIGHT MINERAL OIL (UNII: N6K5787QVP)
ALOE (UNII: V5VD430YW9)
BORNEOL (UNII: M89NIB437X)
CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)
GLYCERIN (UNII: PDC6A3C0OX)
VASICINONE (UNII: G6T5819NXM)
STEMONA JAPONICA ROOT (UNII: FXG254HF10)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)
CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
EUPHORBIA NERIIFOLIA LEAF (UNII: IRZ1UXK5K9)
STEARIC ACID (UNII: 4ELV7Z65AP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-142-01	100 g in 1 BOTTLE; Type 0: Not a Combination Product	02/14/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	02/14/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)