FDA.reportPublic FDA data

LMNOOP

Manufacturer
Shenzhen iShan Technology Co., Ltd
Effective date
2026-02-12
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:37:35

Label at a glance#

ProductLMNOOP
Active ingredientMENTHOL
Label structure11 sections

Dosage and administration

Wash and dry affected area, apply a thin layer of LMNOOP over affected area, Gently massage until fully absorbed, repeat 1-2 times daily

Storage and handling

Store at room temperature, may stain fabric

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Menthol

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children if swallowed, call poison control or seek medical help.

Consulting a doctor before using

OTC - ASK DOCTOR/PHARMACIST SECTION

If pregnant or breast-feeding, ask a health professional before use.

Stop use and ask a doctor

OTC - STOP USE SECTION

if your condition worsens, does not improve, persists for more than 7 days, or occurs again after a few days.

Purpose

OTC - PURPOSE SECTION

Anti-inflammatory, help heal.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature, may stain fabric

Directions

INDICATIONS & USAGE SECTION

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

USER SAFETY WARNINGS SECTION


do not get into eyes. do not apply to wounds or damaged skin. discontinue in case of allergy.

Warnings

WARNINGS SECTION

External use only.

Lable

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

132132

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73076-132-012023-01-30C16284748780-1f386c649-ce18-0266-e053-dadaa90a7c1ad0f718e4-91dd-51d2-e053-2a95a90ae44f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73076-132-01LMNOOP50 g in 1 TUBECREAM503

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73076-13273076-132-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
PHELLODENDRON CHINENSE WHOLEQKA3ZK8IIEIACT
BASSIA SCOPARIA FRUIT04W97Z676YIACT
CNIDIUM MONNIERI FRUITV1IA3S3CUSIACT
STELLERA CHAMAEJASME WHOLE80N0P0DD9JIACT
MENTHOLL7T10EIP3AACTIB
DICTAMNUS DASYCARPUS ROOT6153LEN214IACT
CHLORHEXIDINE ACETATE5908ZUF22YIACT
SOPHORA FLAVESCENS ROOTIYR6K8KQ5KIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LMNOOPMENTHOLShenzhen iShan Technology Co., Ltdd0f718e4-91dd-51d2-e053-2a95a90ae44f2026-02-12WarningsExact identifier
ndc (package): 73076-132-01
ndc (product): 73076-132
ndc11 (package): 73076013201
spl id: 4aadf959-cede-95f1-e063-6394a90a2a4a
spl set id: d0f718e4-91dd-51d2-e053-2a95a90ae44f

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.