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Gembooxt ECZEMA RELIEF Cream drug information

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

Product NDC: 76986-019

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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 nameHYDROCORTISONE
Labeler / manufacturerGuangdong Quadrant Ecological Technology Co., Ltd.
RouteTOPICAL
Drug classCorticosteroid
Product NDC76986-019
Label effective date2026-08-27

Official product label reference

Gembooxt ECZEMA RELIEF Cream — Guangdong Quadrant Ecological Technology Co., Ltd.

This page contains 10 source sections for HYDROCORTISONE, topical route. Label set 46490d65-f789-eaa2-e063-6294a90a623b, 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

Temporarily relieves the itching and discomfort associated with minor skin irritations, rashes, and inflammation, and due to eczema. Other uses of this product should only be under the advice and supervision of a doctor.

Purpose

Anti-ltch
Dosage and administration — label text
Adults and children 2 years of age and older: apply a thin layer to affected area not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor.
Warnings
For external use only.
Active ingredient
Hydrocortisone (1%)
Do not use
Do not use if allergic to any ingredients in this product. Do not use for the treatment of diaper rash. Do not use more than directed unless told to do so by a doctor.
While using this medicine
When using this product, avoid contact with eyes, nose and mouth. lf contact occurs, rinse thoroughly with water. Ask a doctor before use if pregnant or nursing
When to stop use and seek help
Stop using and ask a doctor if condition worsens,symptoms persist for more than 7 days or clear up and occur again within a few days, and do not begin use of any other hydrocortisone product unless you have asked a doctor.
Child safety
Keep out of reach of children. In case of accidental ingestion, get medical help or contact a poison control center immediately.
Inactive ingredient
WATER CETYL ALCOHOL STEARYL ALCOHOL GLYCERYL STEARATE GLYCERIN MINERAL OIL CETEARETH-25 STEARIC ACID ETHYLHEXYL PALMITATE CAMPHOR MENTHOLUM CENTELLA ASIATICA EXTRACT AVENA SATIVA (OAT) KERNEL EXTRACT ROSA RUGOSA FLOWER EXTRACT LACTOBACILLUS FERMENT BUTYLENE GLYCOL DIMETHICONE GLYCERYL CAPRYLATE HYDROXYACETOPHENONE ETHYLHEXYLGLYCERIN 1,2-HEXANEDIOL TRIETHANOLAMINE ALLANTOIN ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER XANTHAN GUM BUTYLENE GLYCOL PENTYLENE GLYCOL HYDROXYPHENYL PROPAMIDOBENZOIC ACID ASCORBYL PALMITATE POTASSIUM LAURYL PHOSPHATE DIPOTASSIUM PHOSPHATE

Official sources and product identifiers

Substances listed: HYDROCORTISONE

RxNorm identifiers: 106258

Package NDC codes

76986-019-01, 76986-019-02

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.