Beaurangcell

Manufacturer
Modoo plan
Effective date
2018-01-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:54:01

Label at a glance#

ProductBeaurangcell
Active ingredientQUERCUS ACUTISSIMA WHOLE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Quercus Acutissima Sap

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice Powder

OTC - PURPOSE SECTION

Skin protection, Skin trouble care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out or reach of the children

INDICATIONS & USAGE SECTION

1) Apply toner to face

2) Apply patch to the desired area

3) After 15-20 min, wipe remove patch and pat the remaining essence.

WARNINGS SECTION

1) Discontinue use or consult dermatologist if irritation, itching or swelling appears after applying the product.

2) Avoid applying patches on the wounded, inflamed or other uncomfortable skin part.

3) Cautions for the storage and handling a) Keep out of children. B) Avoid hot or cold and direct sunlight. c) After unpacking, use the patches immediately to prevent deterioration.

DOSAGE & ADMINISTRATION SECTION

for external use only


PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71962-0001-12020-01-31C16284748780-19d75b9d0-1840-f424-e053-dadaa90a57ce623ef02e-86bb-3a18-e053-2991aa0ad2c6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71962-0001-1Beaurangcell10 mL in 1 POUCHPATCH101
71962-0001-1Beaurangcell10 in 1 PACKAGEPATCH101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71962-0001BEAURANGCELL (QUERCUS ACUTISSIMA SAP) PATCH [MODOO PLAN]1Legacy NDC, 2 package rows20180108_623ef02e-86bb-3a18-e053-2991aa0ad2c6.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71962-000171962-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
QUERCUS ACUTISSIMA WHOLE0TVP714IPWACTIB

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
623ef02e-86bc-3a18-e053-2991aa0ad2c6623ef02e-86bb-3a18-e053-2991aa0ad2c62018-01-08WarningsExact identifier
spl id: 623ef02e-86bc-3a18-e053-2991aa0ad2c6
spl set id: 623ef02e-86bb-3a18-e053-2991aa0ad2c6

Reported adverse events (FAERS/openFDA)#

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