HOUKEA HERBAL NASAL- glycerin spray

HOUKEA Herbal Nasal by

Drug Labeling and Warnings

HOUKEA Herbal Nasal 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

TARAXACUM OFFICINALE、 TURMERIC、 ARTEMISIA VULGARIS ROOT、 SAFFLOWER

PURPOSE

Eliminates mucus to improve breathing; soothes nasal passages to reduce discomfort; sustainably relieves breathing difficulties

USES

1. Clean and dry the nasal cavity.

2. Shake well and open the bottle cap, insert the spray nozzle into the nostril.

3. Spray gently and inhale slowly.

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

INDICATIONS & USAGE

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HOUKEA HERBAL NASAL 
glycerin spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84660-089
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SAFFLOWER (UNII: 4VBL71TY4Y) (SAFFLOWER - UNII:4VBL71TY4Y)	SAFFLOWER	3 mg  in 20 mg
ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S) (ARTEMISIA VULGARIS ROOT - UNII:32MP823R8S)	ARTEMISIA VULGARIS ROOT	3 mg  in 20 mg
TARAXACUM OFFICINALE (UNII: 39981FM375) (TARAXACUM OFFICINALE - UNII:39981FM375)	TARAXACUM OFFICINALE	6 mg  in 20 mg
TURMERIC (UNII: 856YO1Z64F) (TURMERIC - UNII:856YO1Z64F)	TURMERIC	2 mg  in 20 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	6 mg  in 20 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84660-089-01	20 mg 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(84660-089)