Dr Young 2p Brightening UV Sun Block SPF50 PA

Manufacturer: The Doctor's Cosmetic Inc
Effective date: 2009-10-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:23:04

Label at a glance#

ProductDr Young 2p Brightening UV Sun Block SPF50 PA

Active ingredientARBUTIN, OCTINOXATE

Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS:

Hyaluronic Acid, Scutellaria Baicalensis Root Extract, Beta-Glucan, Phytosterols, Arbutin, Octinoxate

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

CAUTION: Keep away from children.

OTC - WHEN USING SECTION

HOW TO USE:

After your basic skin care products, take appropriate amount to put and spread on your entire face.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
43948-5003-1	2019-10-21	C162847	48780-1	956f9ecf-dea2-621f-e053-dbdaa90a74ad	d5915e8d-69ee-486a-9fc9-e35562bf967f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
43948-5003-1	Dr Young 2p Brightening UV Sun Block SPF50 PA	50 mL in 1 TUBE	CREAM	50		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
43948-5003	DR YOUNG 2P BRIGHTENING UV SUN BLOCK SPF50 PA (ARBUTIN, ETHYLHEXYL METHOXYCINNAMATE) CREAM [THE DOCTOR'S COSMETIC INC]	1	Legacy NDC, 1 package rows	20091220_d5915e8d-69ee-486a-9fc9-e35562bf967f.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ARBUTIN	ACTIVE INGREDIENT	C5INA23HXF	1
OCTINOXATE	ACTIVE INGREDIENT	4Y5P7MUD51	1
ARBUTIN	ACTIVE MOIETY	C5INA23HXF	1
OCTINOXATE	ACTIVE MOIETY	4Y5P7MUD51	1

Products#

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

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

Dr Young 2p Brightening UV Sun Block SPF50 PA
ARBUTIN, ETHYLHEXYL METHOXYCINNAMATE
ARBUTIN
OCTINOXATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
43948-5003	43948-5003-1

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
Name	UNII	Kind
ARBUTIN	C5INA23HXF	ACTIB
OCTINOXATE	4Y5P7MUD51	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
0a5ab7a7-8dff-4daf-a586-0689e0b29f6c			d5915e8d-69ee-486a-9fc9-e35562bf967f	2009-10-01		Exact identifier spl id: 0a5ab7a7-8dff-4daf-a586-0689e0b29f6c spl set id: d5915e8d-69ee-486a-9fc9-e35562bf967f

Reported adverse events (FAERS/openFDA)#

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