NATUHEAL RELIEF CREAM FOR ECZEMA- hydrocortisone acetate 1% relief cream for eczema cream

NATUHEAL RELIEF Cream FOR ECZEMA by

Drug Labeling and Warnings

NATUHEAL RELIEF Cream FOR ECZEMA by is a Otc medication manufactured, distributed, or labeled by Jiangxi Yudexi Pharmaceutical Co., LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Active Ingredient 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 Oot 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
■Store at 20°to 25°C(68°to 77°F)
■Protect from excessive heat and direct sunlight

Inactive ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

NATUHEAL RELIEF CREAM FOR ECZEMA 
hydrocortisone acetate 1% relief cream for eczema cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85248-157
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROCORTISONE ACETATE (UNII: 3X7931PO74) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE ACETATE	1 g  in 100 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85248-157-01	20 g in 1 TUBE; Type 0: Not a Combination Product	03/09/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	03/09/2026

Labeler - Jiangxi Yudexi Pharmaceutical Co., LTD (455662836)