Dr.NUELL Brightening Mask Pack

Manufacturer
Apharm Co., Ltd.
Effective date
2019-11-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:01:23

Label at a glance#

ProductDr.NUELL Brightening Mask Pack
Active ingredientGLYCERIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

glycerin

OTC - PURPOSE SECTION

Brightening the dull skin with one sheet mask per day

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

After cleansing, apply mask on clean and towel dried face.

Remove mask after 10 minutes and gently pat excess serum onto face until fully absorbed

WARNINGS SECTION

1) if there is any abnormal symptom or side effect, such as red spot, swelling and itching when using cosmetlcs or after using due to direct sunlight, consult dermatologists
2) Do not use for wounded areas
3) Precautions for storage and handling
keep out of reach of children, store away from direct sunlight
4) avoid the eye area

INACTIVE INGREDIENT SECTION

water, peg-400, sodium hyaluronate, etc.

DOSAGE & ADMINISTRATION SECTION

For external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCERIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73430-0001-12021-01-29C16284748780-1ba0f9c33-14eb-a910-e053-dadaa90a0b8596646b34-b801-41ca-e053-2995a90af75a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73430-0001-1Dr.NUELL Brightening Mask Pack125 mL in 1 PACKAGELIQUID1251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73430-0001DR.NUELL BRIGHTENING MASK PACK (GLYCERIN) LIQUID [APHARM CO., LTD.]1Legacy NDC, 1 package rows20191103_96646b34-b801-41ca-e053-2995a90af75a.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
73430-000173430-0001-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARBUTINC5INA23HXFIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
GLYCERINPDC6A3C0OXACTIB

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
96646b4c-be45-41cc-e053-2995a90a3ad896646b34-b801-41ca-e053-2995a90af75a2019-11-02WarningsExact identifier
spl id: 96646b4c-be45-41cc-e053-2995a90a3ad8
spl set id: 96646b34-b801-41ca-e053-2995a90af75a

Reported adverse events (FAERS/openFDA)#

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