Warnings
For externnl use only.Avoid direct contact with eyes
Ureacream
FDA Label NDC 84019-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shengnan (guangzhou) Cosmetics Co., Ltd for the product Ureacream (NDC 84019-009). 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 warnings, purpose, use section, active ingredient, when using section, inactive ingredient, dosage & administration, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Improves the texture of foot akin, reduicing roughness and making it smoother and more refined.
Use Section
Stop use and ask doctor if rash occurs.
Active Ingredient
Urea 40%
When Using Section
Do not apply to wounds or damaged skin
Inactive Ingredient
Water
Beeswax
Glycerin
Salicylic Acid
Butyrospermum Parkii （Shea） Butter
Dimethicone
Caprylic/Capric Triglyceride
Cetearyl Alcohol
Propylene Glycol
Fragrance
Phenoxyethanol
Palmitic Acid
Stearic Acid
Tocopherol
Panthenol
Dosage & Administration
Apply 1-2 times a day
Indications & Usage
Gently clean the slin let it dry.Apply cream to theafected area. Gendy massage until fullyabsorbed
Package Label.Principal Display Panel
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