FDA.reportPublic FDA data

BY FLOWER BB

Manufacturer
NATURE REPUBLIC CO., LTD.
Effective date
2014-04-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:36:31

Label at a glance#

ProductBY FLOWER BB 01 LIGHT BEIGE
Active ingredientTitanium Dioxide, OCTINOXATE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Titanium Dioxide 9.00%, Ethylhexyl Methoxycinnamate 4.00%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Water, Cyclopentasiloxane, Butylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Cyclohexasiloxane, Glycerin, Silica, Diphenylsiloxy Phenyl Trimethicone, 4-Methylbenzylidene Camphor, Sodium Chloride, Ozokerite, Dimethicone, Butylene Glycol Dicaprylate/Dicaprate,
Arbutin, Dimethicone/Vinyl Dimethicone Crosspolymer, Disteardimonium Hectorite, Quaternium-18 Bentonite, Iron Oxides (CI 77499), Polyglyceryl-4 Isostearate, Iron Oxides (CI 77492), Hexyl Laurate, Iron Oxides (CI 77491), Tocopheryl Acetate, Propylene Carbonate,
Methylparaben, Fragrance, Sorbitan Olivate, Sorbitan Isostearate, Propylparaben, Butylparaben, Beeswax, Panthenol, Calcium Stearate, Echinacea Pallida Extract, Disodium EDTA, Alcohol, Mica (CI 77019), Phenoxyethanol, Sodium Hyaluronate, Centella Asiatica Extract,
Triethoxycaprylylsilane, Ethylhexylglycerin

PURPOSE

OTC - PURPOSE SECTION

Purpose: UV protection, Brightening

Cautions

WARNINGS SECTION

Cautions:
For external use only.
Avoid contact with eyes.
Discontinue use if signs of irritation or rashes appear.
Keep out of reach of children.
Replace the cap after use.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

How to Use

INDICATIONS & USAGE SECTION

How to Use: Apply appropriate amount of B.B. cream onto skin by using fingers or puffs.

How to Use

DOSAGE & ADMINISTRATION SECTION

How to Use: Apply appropriate amount of B.B. cream onto skin by using fingers or puffs.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-247-012020-02-14C16284748780-19d75b9d0-a84f-f424-e053-dadaa90a57ce42280233-866f-4887-bb9d-3bd30b54393b
51346-247-012020-01-31C16284748780-19d75b9d0-a84f-f424-e053-dadaa90a57ce42280233-866f-4887-bb9d-3bd30b54393b

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
Titanium DioxideACTIVE INGREDIENT15FIX9V2JP1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA1
WaterINACTIVE INGREDIENT059QF0KO0R1

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
51346-24751346-247-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
Titanium Dioxide15FIX9V2JPACTIB
OCTINOXATE4Y5P7MUD51ACTIB
Water059QF0KO0RIACT
Butylene Glycol3XUS85K0RAIACT

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
a6db00ba-0108-4592-81f2-2f9b85a6ef9942280233-866f-4887-bb9d-3bd30b54393b2014-04-25WarningsExact identifier
spl id: a6db00ba-0108-4592-81f2-2f9b85a6ef99
spl set id: 42280233-866f-4887-bb9d-3bd30b54393b

Reported adverse events (FAERS/openFDA)#

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