1% KETOCONAZOLE ANTIFUNGAL TREATMENT- antifungal treatment ointment 
Good Manager Holdings Inc

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82372-012 Complete

Active Ingredient

Ketoconazole 1%

Purpose

Antifungal Ointment

Use

1 Treat fungal skin infections such as athlete's foot, jock itch, ringworm, and seborrheic dermatitis.
2. Relieves itching, scaling, and discomfort caused by these fungal infections.

Warnings

For external use only.

Do not use

1. on skin that is broken or inflamed
2. if you are allergic to ingredients in this product

When Using

1. Avoid contact with the eyes
2. If the product gets into eyes, rinse thoroughly with water.

Stop Use

1. if a rash appears or the condition worsens
2. if the condition does not improve in 2-4 weeks.

Ask Doctor

if you are pregnant or breastfeeding.

Keep Oot Of Reach Of Children

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

Directions

Adults and children 12 years and over
1. Apply to the affected area once or twice daily or as directed by a doctor.
2. Wash the affected skin with soap and water and dry completely before applying.
Children under 12 years old. Ask a doctor before use.

Instructions:
1 Clean and dry the affected area before applying the ointment.
2. Apply a small amount of ointment to the affected area and rub in gently.
3. Use daily for up to 4 weeks or as directed by a doctor.

Other information

1. Store at 20°C to 25°C (68°F-77°F)
2. See top panel for lot number and expiration date

Inactive ingredients

Borneol, Sophora Flavescens, Root Cnidium Monnieri, Fruit Kochia, Scopana Pollen, Dictamnus Dasycarpus Root, Smilax Glabra Whole, Artemisia Extract, Tea Tree Oil

Questions

support@tagridllc.com

PRINCIPAL DISPLAY PANEL

1

1% KETOCONAZOLE ANTIFUNGAL TREATMENT 
antifungal treatment ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82372-012
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I) KETOCONAZOLE1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
BASSIA SCOPARIA FRUIT (UNII: 04W97Z676Y)  
SMILAX GLABRA WHOLE (UNII: H51N91QNEB)  
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)  
SCOPINE (UNII: Z5LGM3Q28U)  
BORNEOL (UNII: M89NIB437X)  
WORMWOOD (UNII: F84709P2XV)  
DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)  
TEA TREE OIL (UNII: VIF565UC2G)  
CNIDIUM OFFICINALE ROOT OIL (UNII: 18602BEQ40)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82372-012-0120 g in 1 TUBE; Type 0: Not a Combination Product08/19/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00508/19/202402/12/2025
Labeler - Good Manager Holdings Inc (118382673)
Establishment
NameAddressID/FEIBusiness Operations
Good Manager Holdings Inc118382673label(82372-012)

Revised: 2/2025
 
Good Manager Holdings Inc