76986-019 Gembooxt ECZEMA RELIEF CREAM

Manufacturer
Guangdong Quadrant Ecological Technology Co., Ltd.
Effective date
2026-08-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-01 13:01:56

Label at a glance#

ProductGembooxt ECZEMA RELIEF Cream
Active ingredientHYDROCORTISONE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Hydrocortisone (1%)

OTC - PURPOSE SECTION

Anti-ltch

INDICATIONS & USAGE SECTION


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.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

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.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion, get medical help or contact a poison control center immediately.

DOSAGE & ADMINISTRATION SECTION

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.

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label1label1label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136977863764247GTIN-13: 6977863764247
EAN-13: 6977863764247
GTIN storage (14 digits): 06977863764247
label1.jpg
BarcodeEAN-136977863764254GTIN-13: 6977863764254
EAN-13: 6977863764254
GTIN storage (14 digits): 06977863764254
label1.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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Products#

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

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76986-01976986-019-01, 76986-019-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-12-19full-release2026-06-01 01:26:48

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
Gembooxt ECZEMA RELIEF CreamHYDROCORTISONEGuangdong Quadrant Ecological Technology Co., Ltd.46490d65-f789-eaa2-e063-6294a90a623b2026-08-27WarningsExact identifier
ndc (package): 76986-019-01
ndc (package): 76986-019-02
ndc (product): 76986-019
ndc11 (package): 76986001902
ndc11 (package): 76986001901
spl id: 5a12f61d-6a09-baca-e063-6294a90a4bb1
spl set id: 46490d65-f789-eaa2-e063-6294a90a623b

Reported adverse events (FAERS/openFDA)#

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