Lidothol
Lidothol - Lidocaine HCL 4.5%, Menthol 5% Gel
Approved
Approval ID
f18c6054-3020-64ec-e053-2995a90a57a0
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 10, 2023
Manufacturers
FDA
Advanced Rx Pharmacy of Tennessee, LLC
DUNS: 117023142
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Lidocaine HCL and Menthol
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code80425-0251
Product Classification
G
Generic Name
Lidocaine HCL and Menthol
Product Specifications
Route of AdministrationTOPICAL
Effective DateJanuary 10, 2023
FDA Product Classification
INGREDIENTS (2)
MENTHOLActive
Quantity: 5 g in 100 g
Code: L7T10EIP3A
Classification: ACTIB
LIDOCAINE HYDROCHLORIDEActive
Quantity: 4.5 g in 100 g
Code: V13007Z41A
Classification: ACTIR