Charmpoo Antifungal Cream

Manufacturer
Jiangxi Hemei Pharmaceutical Co., Ltd
Effective date
2025-02-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 20:41:27

Label at a glance#

ProductCharmpoo Antifungal Cream
Active ingredientMICONAZOLE NITRATE
Label structure14 sections

Dosage and administration

1.Clean the affected area and dry it completely. 2.Spread a thin layer of the product onto the affected area twice a day (morningand night) or as your doctor advises. lf your condition doesn't improve, reach out to a doctor. This product is not designed for use on the nails.

Storage and handling

. Do not use if the foil seal at the tube's opening is damaged or absent. . To open the tube: Twist off the cap, lift the tab, and pull to remove the foil seal before using. .Store at room temperature between 10°-30°C(50°-86°F). .Before using any medication, carefullyread all the directions on the label. Retain the carton, as it contains essential information

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Miconazole nitrate 2%

Purpose

OTC - PURPOSE SECTION

Antifungal

Use

INDICATIONS & USAGE SECTION

This product is primarily used to treat skin infections caused by fungi, such as
athlete's foot, jock itch, ringworm, and
tinea versicolor. lt offers rapid relief from symptoms like skin itching, scaling.cracking, burning, and discomfort

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

DO not use on children under 3 years of age unless directed by a doctor.

When Using

OTC - WHEN USING SECTION

When using this product, avoid direct contact with eyes.

Stop Use

OTC - STOP USE SECTION

·lrritation occurs

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

Ask Doctor

OTC - ASK DOCTOR SECTION

·lrritation occurs

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

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

1.Clean the affected area and dry it completely.

2.Spread a thin layer of the product onto the affected area twice a day (morningand night) or as your doctor advises.
lf your condition doesn't improve, reach out to a doctor.

This product is not designed for use on the nails.

Other information

STORAGE AND HANDLING SECTION

. Do not use if the foil seal at the tube's opening is damaged or absent.
. To open the tube: Twist off the cap, lift the tab, and pull to remove the foil seal before using.

.Store at room temperature between 10°-30°C(50°-86°F).

.Before using any medication, carefullyread all the directions on the label. Retain the carton, as it contains essential information

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water, Stearic acid, Medicalvaseline, Glycerin, Vitamin E, Aloe,Stemona, Dictamnus, Sophora Flavescens, Cnidium, Triethanolamine.Chlorhexidine acetate, Euphorbia.Borneol, Natural menthol, Light liquidparaffin.

Questions

OTC - QUESTIONS SECTION

lf you have any questions, please contact us at support@charmpooskincare.com.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84010-069CHARMPOO ANTIFUNGAL CREAM (MICONAZOLE NITRATE 2% ANTIFUNGAL CREAM) CREAM [JIANGXI HEMEI PHARMACEUTICAL CO., LTD]1Unmatched20250212_2dc0f61e-331d-d8b4-e063-6294a90a9152.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84010-06984010-069-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4a4a921c-4245-003c-e063-6294a90a894a2dc0f61e-331d-d8b4-e063-6294a90a91522026-02-08WarningsExact identifier
spl set id: 2dc0f61e-331d-d8b4-e063-6294a90a9152

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.