Active Ingredients
Menthol 7%
Letebee Light Neuropathy Pain Relief Cream For Feet Cream
FDA Label NDC 83566-560
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 Aimu Biological Technology Co., Ltd for the product Letebee Light Neuropathy Pain Relief Cream For Feet (NDC 83566-560). 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, uses, warnings, stop use, do not use, when using, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Pain relieving/Cooling
Uses
Uses for the temporary relief of:tingling burning ·minor foot pain discomfort associated with neuropathy soreness of feet, heels, and toes
Warnings
for external use only. do not bandage tightly.
Stop Use
Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days excessive burning,redness, or irritation occurs
Do Not Use
On open wounds or damaged skin with heating pads or bandages near eyes.mouth, or mucous membranes
When Using
Avoid contact with eyes
Do not use on irritated or broken skin *
Use only as directed
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Get an appropriate amount of Pain Relief Cream with finger and spread evenly on skin.
Inactive Ingredients
WATER 75.35%
PARAFFINUM LIQUIDUM 7%
GLYCERIN 3%
CETEARYL ALCOHOL 2%
GLYCERYL STEARATE 2%
POLYSORBATE 60 1%
SORBITAN STEARATE 1%
POLYACRYLAMIDE 0.25%
C13-14 ISOPARAFFIN 0.25%
LAURETH-7 0.2%
SALVIA MILTIORRHIZA ROOT EXTRACT 0.2%
ANGELICA POLYMORPHA SINENSIS ROOT EXTRACT 0.2%
CENTELLA ASIATICA EXTRACT 0.2%
PHENOXYETHANOL 0.35%
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