Ph.Hubby Pink BB Tone Up Sun

Manufacturer
Ph Hubby Co., Ltd.
Effective date
2022-02-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:07:43

Label at a glance#

ProductPh.Hubby Pink BB Tone Up Sun
Active ingredientADENOSINE, NIACINAMIDE, TITANIUM DIOXIDE, OCTISALATE, BEMOTRIZINOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide, Ethylhexyl Salicylate, Bis-Ethylhexyloxyphenol Methoxyphenyl Triazine, Niacinamide, Adenosine

INACTIVE INGREDIENT SECTION

Water
Butyloctyl Salicylate
C12-15 Alkyl Benzoate
Aluminum Hydroxide
Stearic Acid
Polyglyceryl-6 Polyricinoleate
Dibutyl Adipate
Propanediol
Butylene Glycol
Diethylamino Hydroxybenzoyl Hexyl Benzoate
Polyglyceryl-2 Stearate
Glyceryl Stearate
Stearyl Alcohol

Ethylhexyl Triazone
Water
Triethoxycaprylylsilane
Oleth-10
Polysorbate 60
1,2-Hexanediol
1,2-Hexanediol
Water
Propolis Extract
Propanediol
1,2-Hexanediol
Ethylhexylglycerin
Propanediol
Caprylyl Glycol
Ethylhexylglycerin
Methyl Methacrylate Crosspolymer
Sodium Polyacrylate
Ethylhexyl Stearate
Trideceth-6
Water
Methyl Methacrylate Crosspolymer
Behenyl Alcohol
Musa Sapientum (Banana) Flower Extract
Rosa Damascena Flower Water
Pyrus Communis (Pear) Fruit Extract
Prunus Domestica Fruit Extract
Cucumis Melo (Melon) Fruit Extract
Hedera Helix (Ivy) Leaf/Stem Extract
Eclipta Prostrata Extract
Melia Azadirachta Leaf Extract
Moringa Oleifera Seed Oil
Ammonium Acryloyldimethyltaurate/VP Copolymer
VP/Hexadecene Copolymer
Xanthan Gum

OTC - PURPOSE SECTION

Prevention of hyperpigmentation&aging induced by UVA/UVB rays

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

All year-round. Apply every morning at the end of the skincare routine of going out.

WARNINGS SECTION

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a Doctor if rash or redness occurs

Keep out of reach of children if swallowed, get medical help or contact Poison Control Center right away

Other information

*do not store this product under the direct sun light or the excessive heat

*may stain some fabrics or surfaces

DOSAGE & ADMINISTRATION SECTION

external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82581-0002-12024-03-20C16284748780-10191ceaa-687e-198a-e063-dbdaa90aec3eDrug Facts
82581-0002-12023-07-28C16284748780-10191ceaa-687e-198a-e063-dbdaa90aec3eDrug Facts

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
82581-000282581-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
140fccc5-40b9-d18d-e063-6294a90afbe1d90d17a7-33fe-5cda-e053-2995a90a92442024-03-19WarningsExact identifier
spl set id: d90d17a7-33fe-5cda-e053-2995a90a9244

Reported adverse events (FAERS/openFDA)#

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