XIMONTH SUNFLOWER XANTHIUM SEED OIL- glycerin oil

XIMONTH Sunflower Xanthium Seed Oil by

Drug Labeling and Warnings

XIMONTH Sunflower Xanthium Seed Oil by is a Otc medication manufactured, distributed, or labeled by Guangdong Ouhoe Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

XANTHIUM SIBIRICUM ROOT,HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL,ANGELICA DAHURICA ROOT EXTRACT

purpose

Clear the nasal cavity and relieve nasal discomfort; remove foreign objects blocking the nasal cavity and make the nasal cavity clean and unobstructed; solve acute and chronic rhinitis.

use

Apply an appropriate amount of this product to the affected area and wait for it to be 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.

Do not use

Discontinue use if signs of irritation or rash occur.

Stop 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,LANOLIN

INDICATIONS & USAGE

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

XIMONTH SUNFLOWER XANTHIUM SEED OIL 
glycerin oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84744-052
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
XANTHIUM SIBIRICUM ROOT (UNII: 8555ORT735) (XANTHIUM SIBIRICUM ROOT - UNII:8555ORT735)	XANTHIUM SIBIRICUM ROOT	3 mg  in 10 mg
SUNFLOWER OIL (UNII: 3W1JG795YI) (SUNFLOWER OIL - UNII:3W1JG795YI)	SUNFLOWER OIL	1 mg  in 10 mg
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972) (ANGELICA DAHURICA ROOT - UNII:1V63N2S972)	ANGELICA DAHURICA ROOT	1.5 mg  in 10 mg

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)	3 mg  in 10 mg
GLYCERIN (UNII: PDC6A3C0OX)	1.5 mg  in 10 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84744-052-01	10 mg in 1 BOX; Type 0: Not a Combination Product	10/22/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	10/22/2024

Labeler - Guangdong Ouhoe Biotechnology Co., Ltd. (843651433)

Registrant - Guangdong Ouhoe Biotechnology Co., Ltd. (843651433)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Ouhoe Biotechnology Co., Ltd.		843651433	manufacture(84744-052)