Lycoris Rubus brightening BB

Manufacturer
Lycoris Co., Ltd.
Effective date
2013-10-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:37:08

Label at a glance#

ProductLycoris Rubus brightening BB SPF40 PA Plus Plus
Active ingredientOCTINOXATE, Titanium dioxide, Zinc oxide
Label structure8 sections

Indications and uses

Indications and usage: 1. Tighten the lid after using it. 2. Don’t keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight. 3. Use it in the evening after washing face.

Dosage and administration

Dosage and administration: Apply after washing face. Take a small amount of cream about 1.0-1.5g on to the fingertips and gently massage over the entire face.(cheeks, nostrils, corners, forehead, and the around of eyes, even your hands) Blot face lightly with tissue, and may sleep without washing it.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Ethylhexyl methoxycinnamate 7.5%, Titanium dioxide 5%, Zinc oxide 5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Cyclopentasiloxane, Butylene glycol, Isoamyl p-methoxycinnamate, Cetyl PEG/PPG-10/1 Dimethicone, Betaine, Cetyl ethylhexanoate, Polysorbate 60, Dimethicone, Sodium chloride, Sodium hyaluronate, PEG-40 stearate, Iron oxides, Bentonite, Talc, Stearic acide, Phenoxyethanol, Methylparaben, Ethylparaben, Butylparaben, Propylparaben, Isobutylparaben, Tocopheryl acetate, Perfume, Rubus hirsutus fruit/leaf extract, Camellia Japonica Ovary Powder, Centella asiatica extract, Lavandula angustifolia (Lavender) extract, Glycyrrhiza glabra (Licorice) root extract, Triticum vulgare (Wheat) flour lipids, Allantoin, Lysine HCL, Disodium EDTA, Proline, Sodium ascorbyl phosphate, Linum usitatissimum (Linseed) seed extract, Hibiscus esculentus fruit extract, Aloe barbadensis leaf juice, Arctium lappa root extract, Hibiscus mutabilis flower extract, Corchorus olitorius leaf extract, Dimethyl sulfone

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings: 1. In case of having following symptoms after using this, you’re advised to stop using it immediately. If you keep using it, the symptoms will get worse and need to consult a dermatologist. 1) In case of having problem such as red rash, swollenness, itching, stimulation during usage. 2) In case of having the same symptoms above on the part you put this product on by direct sunlight. 2. You are banned to use it on the part where you have a scar, eczema, or dermatitis. 3. In the case of getting it into your eyes, you have to wash it immediately.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of babies and children

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Indications and usage: 1. Tighten the lid after using it. 2. Don’t keep it in the place where the temperature is extremely hot or low and exposed to the direct sunlight. 3. Use it in the evening after washing face.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

Dosage and administration: Apply after washing face. Take a small amount of cream about 1.0-1.5g on to the fingertips and gently massage over the entire face.(cheeks, nostrils, corners, forehead, and the around of eyes, even your hands) Blot face lightly with tissue, and may sleep without washing it.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ZINC CATION Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809313020147GTIN-13: 8809313020147
EAN-13: 8809313020147
GTIN storage (14 digits): 08809313020147
lycoris rubus brightening bb carton.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
030ce964-9b2d-45aa-b5d3-f78ce03ef61cProduct name220250515
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120
190f2a5b-bbc8-65c7-fcb0-97891307b917Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60778-010-012019-11-27C16284748780-19855e2a2-506d-60a7-e053-dbdaa90a05bd4d78a6bb-2d1f-4ca6-a6f5-37269eb3a4a2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60778-010-01Lycoris Rubus brightening BBSPF40 PA Plus Plus40 mL in 1 CARTONCREAM401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60778-010LYCORIS RUBUS BRIGHTENING BB SPF40 PA PLUS PLUS (OCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE) CREAM [LYCORIS CO., LTD.]1Legacy NDC, 1 package rows20131007_4d78a6bb-2d1f-4ca6-a6f5-37269eb3a4a2.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
Titanium dioxideACTIVE INGREDIENT15FIX9V2JP1
Zinc oxideACTIVE INGREDIENTSOI2LOH54Z1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
ZINC CATIONACTIVE MOIETY13S1S8SF371
Butylene glycolINACTIVE INGREDIENT3XUS85K0RA1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60778-01060778-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Butylene glycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates
Butylene glycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
a81dcd31-a562-47ba-89e5-f9a5cfdcf0c14d78a6bb-2d1f-4ca6-a6f5-37269eb3a4a22013-10-07WarningsExact identifier
spl id: a81dcd31-a562-47ba-89e5-f9a5cfdcf0c1
spl set id: 4d78a6bb-2d1f-4ca6-a6f5-37269eb3a4a2

Reported adverse events (FAERS/openFDA)#

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