MIIN FOOT

Manufacturer
Lydia Co., Ltd. | Aloe Vera Korea Co.,Ltd.
Effective date
2019-08-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:00:08

Label at a glance#

ProductMIIN FOOT
Active ingredientUREA, ALOE VERA LEAF, GLYCERIN, EDETATE DISODIUM
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

urea, glycerin, aloe barbadensis leaf extract, disodium edta

INACTIVE INGREDIENT SECTION

Water, macadamia ternifolia seed oil, stearic acid, shea butter, etc

OTC - PURPOSE SECTION

dead skin cell care cream

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

taking off an appropriate amount

you apply to your rough feet as you massage two or three times a day

WARNINGS SECTION

don’t use on the part where there is injury, eczema, or dermatitis

if swallowed, get medical help or contact a person control center immediately

DOSAGE & ADMINISTRATION SECTION

for topical use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
EDETIC ACID Pharmacologic Class Indexing3Indexing - Pharmacologic Class20180813
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
777d68c6-a5ab-e06c-d314-677b0b9af0c8Product name220240508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72988-0014-12021-01-29C16284748780-1ba0f9c33-1e0b-a910-e053-dadaa90a0b85Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72988-0014-1MIIN FOOT70 g in 1 JARLIQUID701

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72988-0014MIIN FOOT (UREA, GLYCERIN, ALOE, DISODIUM EDTA) LIQUID [LYDIA CO., LTD.]1Legacy NDC, 1 package rows20190823_90beaf4a-3b8d-2d90-e053-2995a90a335e.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72988-001472988-0014-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
90bebc9c-94e6-3bdf-e053-2a95a90a9bb390beaf4a-3b8d-2d90-e053-2995a90a335e2019-08-22WarningsExact identifier
spl id: 90bebc9c-94e6-3bdf-e053-2a95a90a9bb3
spl set id: 90beaf4a-3b8d-2d90-e053-2995a90a335e

Reported adverse events (FAERS/openFDA)#

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