LETEBEE LIGHT NEUROPATHY PAIN RELIEF CREAM FOR FEET- menthol cream

LETEBEE LIGHT neuropathy pain relief cream for feet by

Drug Labeling and Warnings

LETEBEE LIGHT neuropathy pain relief cream for feet by is a Otc medication manufactured, distributed, or labeled by Guangdong Aimu Biological Technology Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredients

Menthol 7%

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%

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LETEBEE LIGHT NEUROPATHY PAIN RELIEF CREAM FOR FEET 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83566-560
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PHENOXYETHANOL (UNII: HIE492ZZ3T)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
PARAFFINUM LIQUIDUM (UNII: T5L8T28FGP)
CENTELLA ASIATICA (UNII: 7M867G6T1U)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
SALVIA MILTIORRHIZA ROOT (UNII: 1693AM5SBN)
POLYSORBATE 60 (UNII: CAL22UVI4M)
LAURETH-7 (UNII: Z95S6G8201)
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
WATER (UNII: 059QF0KO0R)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
ANGELICA POLYMORPHA ROOT (UNII: HZ12173363)
SORBITAN STEARATE (UNII: NVZ4I0H58X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83566-560-01	50 g in 1 JAR; Type 0: Not a Combination Product	12/11/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/11/2025

Labeler - Guangdong Aimu Biological Technology Co., Ltd (712647107)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Aimu Biological Technology Co., Ltd		712647107	manufacture(83566-560)