Dosage & Administration
Apply to affected area twice per day on cleansed skin.
Manuka Honey Foot Cream
FDA Label NDC 84025-087
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Yanxi Biotechnology Co., Ltd for the product Manuka Honey Foot Cream (NDC 84025-087). 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 dosage & administration, warnings, inactive ingredient, indications & usage, otc - keep out of reach of children, otc - purpose, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
keep out of children
Inactive Ingredient
Aqua
Indications & Usage
Craked Heels & Dry Hands
Otc - Keep Out Of Reach Of Children
keep out of children
Otc - Purpose
Improve dryness and cracking Maintain hands and feet& Full body care
Package Label.Principal Display Panel
84025-087 (Fm.2)
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