LETEBEE LIGHT neuropathy pain relief cream for feet

Product NDC
83566-560
11-digit product format
835660560
Labeler code
83566
Product ID
83566-560_45a99afc-15ed-76c2-e063-6294a90a2220
Type
HUMAN OTC DRUG
Nonproprietary name
Menthol
Dosage form
CREAM
Route
TOPICAL
Labeler
Guangdong Aimu Biological Technology Co., Ltd
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-12-11
Substance
MENTHOL
Active strength
7 g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
LETEBEE LIGHT neuropathy pain relief cream for feet
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHOL7 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiL7T10EIP3A
Rxcui2121075

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83566-560-01LETEBEE LIGHT neuropathy pain relief cream for feet50 g in 1 JARCREAM501

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2121075menthol 7 % Topical CreamPSN45a99afc-15ec-76c2-e063-6294a90a22201
2121075menthol 70 MG/ML Topical CreamSCD45a99afc-15ec-76c2-e063-6294a90a22201
2121075menthol 7 % Topical CreamSY45a99afc-15ec-76c2-e063-6294a90a22201

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83566-560-018356605600150 g in 1 JAR (83566-560-01) 50 g2025-12-11NoNoCurrent