Dr Young Protect Prevent Triple Action BB

Manufacturer
Tdc, Co. Ltd | NEW & NEW CO.,LTD.
Effective date
2017-11-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:52:58

Label at a glance#

ProductDr Young Protect Prevent Triple Action BB
Active ingredientTitanium Dioxide, Octinoxate
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: Titanium Dioxide 8.0%, Ethylhexyl Methoxycinnamate 7.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Phenyl Trimethicone, Propylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Arbutin, Cyclopentasiloxane, Hexyl Laurate, Cyclohexasiloxane, Methyl Methacrylate Crosspolymer, Iron Oxides (CI 77492), Glycerin, Magnesium Sulfate, Sorbitan Sesquioleate, Zinc stearate, Caprylyl Methicone, Dimethicone, Microcrystalline Wax, Ozokerite, Isostearyl Isostearate, Polyglyceryl-4 Isostearate, Iron Oxides (CI 77491), Iron Oxides (CI 77499), Quaternium-18 Bentonite, Dimethicone/Vinyl Dimethicone Crosspolymer, Phenoxyethanol, Triethoxycaprylylsilane, Sodium Chloride, Silica Dimethyl Silylate, PEG/PPG-19/19 Dimethicone, Phellinus Linteus Extract, Cyclotetrasiloxane, Caprylyl Glycol, Butylene Glycol, Portulaca Oleracea Extract, Allantoin, Hydroxyethylcellulose, Ultramarines(CI 77007), Centella Asiatica Extract, Piper Methysticum Leaf/Root/Stem Extract, Adenosine, Caprylhydroxamic Acid, Petrolatum, Tocopheryl Acetate, Mica, Polysilicone-11, Aloe Barbadensis Leaf Juice, Lilium Candidum Bulb Extract, Iris Versicolor Extract, Freesia Alba Flower Extract, Narcissus Pseudo-Narcissus (Daffodil) Flower Extract, Rosa Damascena Flower Water, Leontopodium Alpinum Extract, Nelumbo Nucifera Flower Extract, Jasminum Officinale (Jasmine) Flower/Leaf Extract

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warning: 1) For external use only. 2) Consult a dermatologist if the first sign occurs like red spot, swelling, itching, or any allergic reactions. 3) Avoid direct contact with eyes. 4) If contact occurs, flush thoroughly with water. 5) If swallowed, get medical help or contact a Poison Control Center right away. 6) Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

Storage and cautions for handling: 1) Keep out of reach of children. 2) Keep away from high or low temperature and direct sunlight.

DESCRIPTION

DESCRIPTION SECTION

Uses: - Ultralight, Multifunctional beauty cream to protect, perfect, tint, and moisturize skin - Features SPF 33 PA+++ sun protection

Directions: Apply moderate amount on entire face after basic skin care.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43948-1330-22020-01-31C16284748780-19d75b9cf-ead7-f424-e053-dadaa90a57cedc1979a5-f36a-4a8f-a2e5-7d3443eb2d6c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43948-1330-1Dr Young Protect Prevent Triple Action BB30 mL in 1 TUBECREAM301
43948-1330-2Dr Young Protect Prevent Triple Action BB1 in 1 CARTONCREAM11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43948-1330DR YOUNG PROTECT PREVENT TRIPLE ACTION BB (TITANIUM DIOXIDE, OCTINOXATE) CREAM [TDC, CO. LTD]1Legacy NDC, 2 package rows20171114_dc1979a5-f36a-4a8f-a2e5-7d3443eb2d6c.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43948-133043948-1330-1, 43948-1330-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
a443b0a1-b275-4fb8-bb24-16b4b5e98095dc1979a5-f36a-4a8f-a2e5-7d3443eb2d6c2017-11-14WarningsExact identifier
spl id: a443b0a1-b275-4fb8-bb24-16b4b5e98095
spl set id: dc1979a5-f36a-4a8f-a2e5-7d3443eb2d6c

Reported adverse events (FAERS/openFDA)#

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