LMNOOP Seborrheic Dermatitis Treatment

Manufacturer
Shenzhen Ishan Technology Co., Ltd
Effective date
2026-02-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:37:31

Label at a glance#

ProductLMNOOP Seborrheic Dermatitis Treatment
Active ingredientOATMEAL
Label structure11 sections

Indications and uses

Anti-bacterial, reduces itchy and painful skin conditions due to eczema, athletes foot, psoriasis, jock itch, rash, skin yeast infection and more.

Dosage and administration

Wash and dry affected area, apply a thin layer of LMNOOP over affected area, gently massage until fully absorbed, repeat 2-3 times daily.

Storage and handling

Store at room temperature.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Colloidal Oatmeal--1%--Skin protectant.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purify water, dictamnus dasycarpus root, stellera chamaejasme whole, sophora flavescens root, cnidium monnieri fruit, phellodendron chinense whole, bassia scoparia fruit, Menthol.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

if swallowed, call poison control or seek medical help.

Ask a doctor

OTC - ASK DOCTOR/PHARMACIST SECTION

before using on children under 2 years of age.

Stop use

OTC - STOP USE SECTION

if condition worsens, symptoms last more than 7 days or clear up and occur again within a few days, or there is no improvement of athlete's foot or psoriasis within 4 weeks or jock itch with 2 weeks.

Uses

OTC - PURPOSE SECTION

Anti-bacterial, reduces itchy and painful skin conditions due to eczema, athletes foot, psoriasis, jock itch, rash, skin yeast infection and more.

Other information

STORAGE AND HANDLING SECTION

Store at room temperature.

Directions

INDICATIONS & USAGE SECTION

Wash and dry affected area, apply a thin layer of LMNOOP over affected area, gently massage until fully absorbed, repeat 2-3 times daily.

When using this product

USER SAFETY WARNINGS SECTION

o not get into eyes. do not apply to wounds or damaged skin.

Warnings

WARNINGS SECTION

For external only

Lable

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136973496921507GTIN-13: 6973496921507
EAN-13: 6973496921507
GTIN storage (14 digits): 06973496921507
LMNOOP Seborrheic.jpg
QR code linkQR Codewww.lmnoop.com/LMNOOP Seborrheic.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73076-203-012026-01-29C16284748780-149896155-c149-586f-e063-e6dba90add901a0eb78f-e915-b4fe-e063-6394a90a7fe0
73076-203-022026-01-29C16284748780-149896155-c149-586f-e063-e6dba90add901a0eb78f-e915-b4fe-e063-6394a90a7fe0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73076-203-01LMNOOP Seborrheic Dermatitis Treatment50 g in 1 PACKAGECREAM503
73076-203-02LMNOOP Seborrheic Dermatitis Treatment100 g in 1 BOTTLECREAM1003

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73076-20373076-203-01, 73076-203-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

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
LMNOOP Seborrheic Dermatitis TreatmentLMNOOP SEBORRHEIC DERMATITIS TREATMENTShenzhen Ishan Technology Co., Ltd1a0eb78f-e915-b4fe-e063-6394a90a7fe02026-02-13WarningsExact identifier
ndc (package): 73076-203-02
ndc (package): 73076-203-01
ndc (product): 73076-203
ndc11 (package): 73076020302
ndc11 (package): 73076020301
spl id: 4aae9189-a382-7614-e063-6394a90a8420
spl set id: 1a0eb78f-e915-b4fe-e063-6394a90a7fe0

Reported adverse events (FAERS/openFDA)#

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