Dr.LIBEAUTE Multi-Purpose Cleansing Wipes

Manufacturer
Ongoong Co Ltd
Effective date
2020-08-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:24:49

Label at a glance#

ProductDr.LIBEAUTE Multi-Purpose Cleansing Wipes
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ethyl alcohol

INACTIVE INGREDIENT SECTION

Water,Sodium Benzoate,Polysorbate 20,Caprylyl Glycol,Ethylhexylglycerin,Dipropylene Glycol,Glycerin,Glyceryl Caprylate,Citric Acid,Disodium EDTA,Camellia Sinensis Leaf Extract,Butylene Glycol,Aloe Barbadensis Leaf Extract,fragrance.

OTC - PURPOSE SECTION

cleansing hands and all kinds of surfaces

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

open package lid, completely remove inner seal, apply pressure around opening and pull wipe out

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74084-0010-12023-01-30C16284748780-1f386c649-9d0a-0266-e053-dadaa90a7c1aDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74084-0010-1Dr.LIBEAUTE Multi-Purpose Cleansing Wipes450 g in 1 PACKAGELIQUID4501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74084-0010DR.LIBEAUTE MULTI-PURPOSE CLEANSING WIPES (ALCOHOL) LIQUID [ONGOONG CO LTD]1Legacy NDC, 1 package rows20200815_acdf391d-01b9-e6ac-e053-2995a90a1593.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
74084-001074084-0010-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
acdf28a2-65aa-daf0-e053-2a95a90a1cf3acdf391d-01b9-e6ac-e053-2995a90a15932020-08-14WarningsExact identifier
spl id: acdf28a2-65aa-daf0-e053-2a95a90a1cf3
spl set id: acdf391d-01b9-e6ac-e053-2995a90a1593

Reported adverse events (FAERS/openFDA)#

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