Dr.NUELL Multi Sun Block

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 Multi Sun Block
Active ingredientZINC OXIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

zinc oxide

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

before foundation BB cream, apply it as a substitute for a primer.

if the foundation you use is dark, mix it with a small amount of sun block to adjust the tone before use

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, butylene glycol, cyclopentasiloxane, etc.

DOSAGE & ADMINISTRATION SECTION

For external use only

OTC - PURPOSE SECTION

dual functionality for brightening and wrinkle improvement certified

OTC - PURPOSE SECTION

mild UV protection without irritation SPF 42, PA+++

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73430-0005-12021-01-29C16284748780-1ba0f9c33-3381-a910-e053-dadaa90a0b85966d70e7-06a6-cd69-e053-2a95a90a2ab3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73430-0005-1Dr.NUELL Multi Sun Block50 mL in 1 BOTTLECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73430-0005DR.NUELL MULTI SUN BLOCK (ZINC OXIDE) CREAM [APHARM CO., LTD.]1Legacy NDC, 1 package rows20191103_966d70e7-06a6-cd69-e053-2a95a90a2ab3.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
73430-000573430-0005-1

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
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ZINC OXIDESOI2LOH54ZACTIB

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
966d70e7-06a7-cd69-e053-2a95a90a2ab3966d70e7-06a6-cd69-e053-2a95a90a2ab32019-11-03WarningsExact identifier
spl id: 966d70e7-06a7-cd69-e053-2a95a90a2ab3
spl set id: 966d70e7-06a6-cd69-e053-2a95a90a2ab3

Reported adverse events (FAERS/openFDA)#

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