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OTC products · Product label record

Gembooxt Ketoconazole 1% Medicated Shampoos drug information

KETOCONAZOLE
Guangdong Quadrant Ecological Technology Co., Ltd. · TOPICAL

Product NDC: 76986-025

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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 nameKETOCONAZOLE
Labeler / manufacturerGuangdong Quadrant Ecological Technology Co., Ltd.
RouteTOPICAL
Drug classAzole Antifungal
Product NDC76986-025
Label effective date2026-08-27

Official product label reference

Gembooxt Ketoconazole 1% Medicated Shampoos — Guangdong Quadrant Ecological Technology Co., Ltd.

This page contains 10 source sections for KETOCONAZOLE, topical route. Label set 49965e91-43c3-65d7-e063-6294a90abaec, 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

Controls flaking, scaling and itching associated with dandruff

Purpose

Anti-dandruff shampoo
Dosage and administration — label text
For adults and children 12 years and older: 1. Wet hair thoroughly. 2. Apply shampoo, generously lather, rinse thoroughly. Repeat. 3. Use every 3-4 days for up to 8 weeks or as directed by a doctor.Then use only as needed to control dandruff. Children under 12 years: Ask a doctor.
Warnings
For external use only.
Active ingredient
Ketoconazole 1%
Do not use
on scalp that is broken or inflamed. if you are allergic to ingredients in this product.
While using this medicine
When using this products. Avoid contact with eyes. lf contact occurs, rinse thoroughly with water. If pregnant or breast-feeding, ask a doctor before use.
When to stop use and seek help
rash appears. condition worsens or does not improve in 2-4 weeks.
Child safety
Keep out of reach of children. lf swallowed, get medical help or contact a Poison Control Center right away.
Inactive ingredient
WATER SODIUM LAUROYL SARCOSINATE COCAMIDOPROPYL BETAINE WATER PARFUM GLYCERYL CAPRYLATE GLYCERYL LAURATE PHENOXYETHANOL WATER LAURYL LACTATE CITRIC ACID POLYQUATERNIUM-10 DISODIUM EDTA HYDROLYZED RHODOPHYCEAE EXTRACT BUTYLENE GLYCOL 1,2-HEXANEDIOL PENTYLENE GLYCOL PROPANEDIOL CAPRYLHYDROXAMIC ACID ETHYLHEXYLGLYCERIN BIOTIN POTASSIUM HYDROXIDE

Official sources and product identifiers

Substances listed: KETOCONAZOLE

RxNorm identifiers: 240812

Package NDC codes

76986-025-01, 76986-025-02, 76986-025-03

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.