Dr.NUELL Propolis Real 90 Ampoule

Manufacturer
Apharm Co., Ltd.
Effective date
2019-11-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:01:24

Label at a glance#

ProductDr.NUELL Propolis Real 90 Ampoule
Active ingredientGLYCERIN
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

glycerin

OTC - PURPOSE SECTION

a multi ampoule for high-moisturizing & high-nourishing

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

Please refer to the instructions on the package.

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

butylene glycol, sodium hyaluronate, arginine, 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
73430-0004-12021-01-29C16284748780-1ba0f9c33-14ee-a910-e053-dadaa90a0b85966d1783-cada-92cb-e053-2995a90a7db4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73430-0004-1Dr.NUELL Propolis Real 90 Ampoule100 mL in 1 PACKAGELIQUID1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73430-0004DR.NUELL PROPOLIS REAL 90 AMPOULE (GLYCERIN) LIQUID [APHARM CO., LTD.]1Legacy NDC, 1 package rows20191103_966d1783-cada-92cb-e053-2995a90a7db4.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
73430-000473430-0004-1

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
ALLANTOIN344S277G0ZIACT
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
966d1a82-c8c2-9795-e053-2995a90a0a71966d1783-cada-92cb-e053-2995a90a7db42019-11-03WarningsExact identifier
spl id: 966d1a82-c8c2-9795-e053-2995a90a0a71
spl set id: 966d1783-cada-92cb-e053-2995a90a7db4

Reported adverse events (FAERS/openFDA)#

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