SERYNTH ECZEMA RELIEF by Jiangxi Hemei Pharmaceutical Co., Ltd 84010-152complete

SERYNTH ECZEMA RELIEF by

Drug Labeling and Warnings

SERYNTH ECZEMA RELIEF by is a Otc medication manufactured, distributed, or labeled by Jiangxi Hemei Pharmaceutical Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SERYNTH ECZEMA RELIEF- hydrocortisone 1% eczema relief cream 
Jiangxi Hemei Pharmaceutical Co., Ltd

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84010-152complete

Active Ingredient

Hydrocortisone 1%

Purpose

Anti-itch

Use

■temporarily relieves 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

■for the treatment of diaper rash. Consult a doctor.

When Using

■avoid contact with eyes

■do not use more than directed unless told to do so by a doctor

Stop Use

■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

Ask Doctor

■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

If swallowed, get medical help or contact a Poison Control Center right away

Directions

■adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
■children under 2 years of age: ask a doctor

Other information

■contents filled by weight, not volume

Inactive ingredients

Cetyl Alcohol, Glycerin, Avena sativa (oat) kernel extract, Bisabolol, Glyceryl stearate,Isohexadecane,Magnesium ascorbyl phosphate, Maltodextrin, Borneol, Menthol

PRINCIPAL DISPLAY PANEL

SERYNTH ECZEMA RELIEF 
hydrocortisone 1% eczema relief cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84010-152
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CETYL ALCOHOL (UNII: 936JST6JCN)
GLYCERYL 1-STEARATE (UNII: 258491E1RZ)
ISOHEXADECANE (UNII: 918X1OUF1E)
BISABOLOL (UNII: 24WE03BX2T)
MENTHOL (UNII: L7T10EIP3A)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
BORNEOL (UNII: M89NIB437X)
OAT (UNII: Z6J799EAJK)
MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84010-152-01	20 g in 1 TUBE; Type 0: Not a Combination Product	07/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	07/15/2025	02/08/2026

Labeler - Jiangxi Hemei Pharmaceutical Co., Ltd (724892056)

Establishment
Name	Address	ID/FEI	Business Operations
Jiangxi Hemei Pharmaceutical Co., Ltd		724892056	manufacture(84010-152)

Revised: 2/2026

Document Id: 4a4c8d5b-f947-1eb8-e063-6394a90a8d39

34390-5

Set id: 39f7c0f9-5f3e-b9b8-e063-6394a90ae965

Version: 2

Effective Time: 20260208