SUPER BB

Manufacturer: UNHWA CORPORATION
Effective date: 2010-05-20
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-05-31 22:24:34

Label at a glance#

ProductSUPER BB ANTI WRINKLE AND SUN PROTECTION SPF36

Active ingredientTITANIUM DIOXIDE

Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: TITANIUM DIOXIDE

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Dipropylene Glycol, Cyclopentasiloxane, Ethylhexyl Methoxycinnamate, Panax Ginseng Cambium Cell Culture Extract, Polysilicone-11, Dimethicone Crosspolymer, Glycerin, Hexyl Laurate, Pentaerythrityl Tetraethylhexanoate, Isoamyl p-Methoxycinnamate, Dimethicone, Magnesium Sulfate, Disteardimonium Hectorite, Cetyl PEG/PPG-10/1 Dimethicone, PEG-10 Dimethicone, Sorbitan Sesquioleate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Beeswax, Panthenol, Talc, Phenoxyethanol, Palmitoyl Oligopeptide, Phaseolus Radiatus Seed Extract, Cornus Officinalis Fruit Extract, Aloe Arborescens Leaf Extract, Methylparaben, Triethoxycaprylylsilane, Propylparaben, Ethyl paraben, Glyceryl Polymethacrylate, Propylene Glycol, Adenosine, Alcohol, Iron Oxides(Yellow), Iron Oxides(Red), Iron Oxides(Black), Fragrance

DESCRIPTION SECTION

Direction for Use: Place a small amount on fingertip. Lightly pat and smooth evenly on face and neck.
Storage: Store in cool and dry place.
Warning: For external use only. Should any abnormality appear, stop usage of the product and consult doctor.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
50556-001-01	2019-10-21	C162847	48780-1	956f9ecf-d21e-621f-e053-dbdaa90a74ad	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50556-001-01	SUPER BBANTI WRINKLE AND SUN PROTECTION SPF36	30 mL in 1 CARTON	CREAM	30		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50556-001	SUPER BB ANTI WRINKLE AND SUN PROTECTION SPF36 (TITANIUM DIOXIDE) CREAM [UNHWA CORPORATION]	7	Legacy NDC, 1 package rows	20100521_1b4ce6a8-51ab-448e-b63f-ea72a8e02a08.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
TITANIUM DIOXIDE	ACTIVE INGREDIENT	15FIX9V2JP	7
TITANIUM	ACTIVE MOIETY	D1JT611TNE	7

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

SUPER BB ANTI WRINKLE AND SUN PROTECTION SPF36
TITANIUM DIOXIDE
TITANIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50556-001	50556-001-01

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
Name	UNII	Kind
TITANIUM DIOXIDE	15FIX9V2JP	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
9ebea00c-ffd4-47cb-afb8-189b0e1ba705			1b4ce6a8-51ab-448e-b63f-ea72a8e02a08	2010-05-20		Exact identifier spl id: 9ebea00c-ffd4-47cb-afb8-189b0e1ba705 spl set id: 1b4ce6a8-51ab-448e-b63f-ea72a8e02a08

Reported adverse events (FAERS/openFDA)#

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