Dr Young 2p Blemish Base SPF35 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 22:22:55

Label at a glance#

ProductDr Young 2p Blemish Base SPF35 PA
Active ingredientALLANTOIN
Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS:

Chrysanthellum Indicum Extract, Butyrospermum ParkII (Shea Butter), Magnolia Kobus Bark Extract, Camellia Sinensis Leaf Extract, Citrus Grandis (Grapefruit) Fruit Extract, Centella Asiatica Extract, Althaea Rosea Flower Extract, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate, Allantoin, Ceramide 3

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


Label12c


LABELLABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43948-5001-12019-10-21C16284748780-1956f9ecf-d656-621f-e053-dbdaa90a74ada0df0a17-38ee-4750-a761-3d718f62f3f7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43948-5001-1Dr Young 2p Blemish Base SPF35 PA60 mL in 1 TUBECREAM601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43948-5001DR YOUNG 2P BLEMISH BASE SPF35 PA (ALLANTOIN) CREAM [THE DOCTOR'S COSMETIC INC]1Legacy NDC, 1 package rows20091208_a0df0a17-38ee-4750-a761-3d718f62f3f7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALLANTOINACTIVE INGREDIENT344S277G0Z1
ALLANTOINACTIVE MOIETY344S277G0Z1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43948-500143948-5001-1

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
ALLANTOIN344S277G0ZACTIB

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
7dc42f89-3624-47b8-9092-a89408e467eca0df0a17-38ee-4750-a761-3d718f62f3f72009-10-01Exact identifier
spl id: 7dc42f89-3624-47b8-9092-a89408e467ec
spl set id: a0df0a17-38ee-4750-a761-3d718f62f3f7

Reported adverse events (FAERS/openFDA)#

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