GEMBOOXT ECZEMA RELIEF CREAM- hydrocortisone cream

Gembooxt ECZEMA RELIEF Cream by

Drug Labeling and Warnings

Gembooxt ECZEMA RELIEF Cream by is a Otc medication manufactured, distributed, or labeled by Guangdong Quadrant Ecological Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Hydrocortisone (1%)

PURPOSE

Anti-ltch

INDICATIONS & USAGE

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

For external use only.

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.

WHEN USING

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

STOP USE

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.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

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

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GEMBOOXT ECZEMA RELIEF CREAM 
hydrocortisone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76986-019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	0.01 g  in 1 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CETEARETH-25 (UNII: 8FA93U5T67)
DIMETHICONE (UNII: 92RU3N3Y1O)
DIBASIC POTASSIUM PHOSPHATE (UNII: CI71S98N1Z)
HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
XANTHAN GUM (UNII: TTV12P4NEE)
STEARIC ACID (UNII: 4ELV7Z65AP)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
ROSA RUGOSA FLOWER (UNII: 969IQC5YJU)
ASCORBYL PALMITATE (UNII: QN83US2B0N)
POTASSIUM LAURYL PHOSPHATE (UNII: C4QT53N4MK)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
CETYL ALCOHOL (UNII: 936JST6JCN)
ALLANTOIN (UNII: 344S277G0Z)
OAT (UNII: Z6J799EAJK)
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ETHYLHEXYL PALMITATE (UNII: 2865993309)
MINERAL OIL (UNII: T5L8T28FGP)
MENTHOL (UNII: L7T10EIP3A)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S AT 0.5%) (UNII: YY2HMJ9NZF)
GLYCERIN (UNII: PDC6A3C0OX)
LACTOBACILLUS REUTERI F275 STRAIN (UNII: 3K209OP33H)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76986-019-01	2 in 1 BOX	12/19/2025
1		15 g in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 76986-019-02	20 in 1 BOX	12/19/2025
2		1.5 g in 1 BAG; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	12/19/2025

Labeler - Guangdong Quadrant Ecological Technology Co., Ltd. (554532634)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Quadrant Ecological Technology Co., Ltd.		554532634	manufacture(76986-019)