XIMONTH XANTHIUM SEED OIL NOSE HEALTH CARE SOLUTION- glycerin liquid

XIMONTH Xanthium Seed Oil Nose Health Care Solution by

Drug Labeling and Warnings

XIMONTH Xanthium Seed Oil Nose Health Care Solution 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、SUNFLOWER OIL、ANGELICA DAHURICA ROOT

purpose

Clear the nasal cavity andeliee aremove foreign objectsblocking the nasal cavityand make the nasal cavityclean and unobstructed;solve acute and chronicrhinitis.

use

Drop an appropriate amount of this product on a cotton swab and apply it to the entire nasal cavity. Wait for it to be absorbed and then remove the cotton swab.

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 XANTHIUM SEED OIL NOSE HEALTH CARE SOLUTION 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84744-053
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	9 mg  in 30 mg
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972) (ANGELICA DAHURICA ROOT - UNII:1V63N2S972)	ANGELICA DAHURICA ROOT	4.5 mg  in 30 mg
SUNFLOWER OIL (UNII: 3W1JG795YI) (SUNFLOWER OIL - UNII:3W1JG795YI)	SUNFLOWER OIL	3 mg  in 30 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	4.5 mg  in 30 mg
LANOLIN (UNII: 7EV65EAW6H)	9 mg  in 30 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84744-053-01	30 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(84744-053)