Active Ingredients
Menthol
Lmnoop Cream
FDA Label NDC 73076-132
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Ishan Technology Co., Ltd for the product Lmnoop (NDC 73076-132). 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, inactive ingredients, keep out of reach of children, consulting a doctor before using, stop use and ask a doctor, purpose, other information, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredients
STELLERA CHAMAEJASME WHOLE
DICTAMNUS DASYCARPUS ROOT
BASSIA SCOPARIA FRUIT
CNIDIUM MONNIERI FRUIT
SOPHORA FLAVESCENS ROOT
PHELLODENDRON CHINENSE WHOLE
CHLORHEXIDINE ACETATE
Keep Out Of Reach Of Children
Keep out of reach of children if swallowed, call poison control or seek medical help.
Consulting A Doctor Before Using
If pregnant or breast-feeding, ask a health professional before use.
Stop Use And Ask A Doctor
if your condition worsens, does not improve, persists for more than 7 days, or occurs again after a few days.
Purpose
Anti-inflammatory, help heal.
Other Information
Store at room temperature, may stain fabric
Directions
Wash and dry affected area, apply a thin layer of LMNOOP over affected area, Gently
massage until fully absorbed, repeat 1-2 times daily
When Using This Product
do not get into eyes. do not apply to wounds or damaged skin. discontinue in case of allergy.
Warnings
External use only.
* Please review the disclaimer below.
