HOUKEA SEBORRHEIC DERMATITIS- glycerin spray

HOUKEA Seborrheic Dermatitis by

Drug Labeling and Warnings

HOUKEA Seborrheic Dermatitis by is a Otc medication manufactured, distributed, or labeled by Guangdong Ximonth Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

MENTHA PIPERITA LEAF、SHEA BUTTER、TOCOPHEROL

PURPOSE

Relieve seborrheic dermatitis symptoms; soothe skin redness and discomfort; calm skin itching and discomfort

USES

Clean your scalp and facial skin and keep them dry. Spray this product evenly on the affected areas of dermatitis on your scalp and face, and massage until absorbed.

WARNINGS

Please keep out of reach of children. Do not swallow.Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.

STOP USE

Discontinue use if signs of irritation or rash occur.

DO NOT USE

Discontinue use if signs of irritation or rash occur.

KEEP OUT OF REACH OF CHILDREN

Please keep out of reach of children. Do not swallow.

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

GLYCERIN、ALLANTOIN

INDICATIONS & USAGE

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HOUKEA SEBORRHEIC DERMATITIS 
glycerin spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84660-096
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHA PIPERITA LEAF (UNII: A389O33LX6) (MENTHA PIPERITA LEAF - UNII:A389O33LX6)	MENTHA PIPERITA LEAF	9 g  in 30 g
SHEA BUTTER (UNII: K49155WL9Y) (SHEA BUTTER - UNII:K49155WL9Y)	SHEA BUTTER	3 g  in 30 g
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8)	TOCOPHEROL	4.5 g  in 30 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	4.5 g  in 30 g
ALLANTOIN (UNII: 344S277G0Z)	9 g  in 30 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84660-096-01	30 g in 1 BOX; Type 0: Not a Combination Product	10/29/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M014	10/29/2024

Labeler - Guangdong Ximonth Technology Co., Ltd. (699436264)

Registrant - Guangdong Ximonth Technology Co., Ltd. (699436264)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Ximonth Technology Co., Ltd.		699436264	manufacture(84660-096)