Active Ingredients
XANTHIUM SIBIRICUM ROOT,HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL,ANGELICA DAHURICA ROOT EXTRACT
Ximonth Sunflower Xanthium Seed Oil
FDA Label NDC 84744-052
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Ouhoe Biotechnology Co., Ltd. for the product Ximonth Sunflower Xanthium Seed Oil (NDC 84744-052). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, use, warnings, do not use, stop use, otc - keep out of reach of children, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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.
Otc - 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
Package Label.Principal Display Panel
Label (Xi B03 0094 01)
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