Active Ingredient(S)
SALIX ALBA BARK、FRANKINCENSE、ARNICA MONTANA FLOWER
Houkea Bone Pain Treatment Cream
FDA Label NDC 84660-100
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�ximonth�technology�co.,�ltd. for the product Houkea Bone Pain Treatment Cream (NDC 84660-100). 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 ingredient(s), purpose, use, warnings, do not use, stop use, otc - keep out of reach of children, safe handling warning, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Quickly relieve bone and joint discomfort; improve local blood circulation; improve joint mobility.
Use
1. Clean and dry skin.
2. Take an appropriate amount of this product and apply it evenly on the affected area.
3. Massage gently 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.
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.
Safe Handling Warning
Store in a cool and dry place.
Inactive Ingredient
GLYCERIN、DIMETHYL SULFONE
Package Label.Principal Display Panel
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Package Label (Hk B04 0014 01(1))
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