FDA.reportPublic FDA data

Be Beautiful Pure Make Up Base Purple

Manufacturer
THANK YOU FARMER CO., LTD. | Kolmar Korea Co., Ltd.
Effective date
2018-11-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:47:57

Label at a glance#

ProductBe Beautiful Pure Make Up Base Purple
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Octinoxate 6.00% …………………………………Sunscreen
Titanium Dioxide 4.02% ..………………..……Sunscreen
Octisalate 2.00% ……………………....…………Sunscreen
Zinc Oxide 1.92% ………………………………….Sunscreen

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Helps prevent sunburn

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure. Reapply at least every two hours


Sun protection measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 of higher and other sun protection measures including: 1) Limited time in the sun, especially from 10 am to 2 pm. 2) Wear long-sleeve shirts, pants, hats, and sunglasses

Ask a doctor to use for children under 6 months

WARNINGS SECTION

For external use only

Do not use on damaged or broken skin

Stop using and ask a doctor if rash occurs

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

INACTIVE INGREDIENT SECTION

WATER, CYCLOPENTASILOXANE, BUTYLENE GLYCOL, PHENYL TRIMETHICONE, ISOEICOSANE, CAPRYLYL METHICONE, PEG-10 DIMETHICONE, DIMETHICONE, NIACINAMIDE, ULTRAMARINES (CI 77007), DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, DIMETHICONE CROSSPOLYMER, TALC, C12-14 PARETH-3, PHENOXYETHANOL, FRAGRANCE, PALMITIC ACID, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, METHICONE, ETHYLHEXYLGLYCERIN, TOCOPHERYL ACETATE, OCTYLDODECANOL, ADENOSINE, SODIUM HYALURONATE, ECHIUM PLANTAGINEUM SEED OIL, CARDIOSPERMUM HALICACABUM FLOWER/LEAF/VINE EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLES, TOCOPHEROL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70618-008-022024-03-26C16284748780-1d6a99b39-d0eb-a426-e053-dadaa90af4c2Drug Facts
70618-008-022022-01-28C16284748780-1d6a99b39-d0eb-a426-e053-dadaa90af4c2Drug Facts

Products#

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

DailyMed product names page 1 of 1 · 35 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70618-00870618-008-01, 70618-008-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CYCLOMETHICONE 50THT5PCI0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
PHENYL TRIMETHICONEDR0K5NOJ4RIACT
ISOEICOSANEAR294KAG3TIACT
CAPRYLYL TRISILOXANEQ95M2P1KJLIACT
PEG-10 DIMETHICONE (600 CST)8PR7V1SVM0IACT
DIMETHICONE92RU3N3Y1OIACT
NIACINAMIDE25X51I8RD4IACT
ULTRAMARINE BLUEI39WR998BIIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
MAGNESIUM SULFATE, UNSPECIFIED FORMDE08037SABIACT
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER9NH1UDD2RRIACT
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)UF7620L1W6IACT
TALC7SEV7J4R1UIACT
C12-14 PARETH-393RY22U87EIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PALMITIC ACID2V16EO95H1IACT
ALUMINUM HYDROXIDE5QB0T2IUN0IACT
ALUMINUM STEARATEU6XF9NP8HMIACT
METHICONE (20 CST)6777U11MKTIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
OCTYLDODECANOL461N1O614YIACT
ADENOSINEK72T3FS567IACT
HYALURONATE SODIUMYSE9PPT4THIACT
ECHIUM PLANTAGINEUM SEED OILPIB7XBU8XWIACT
TOCOPHEROLR0ZB2556P8IACT
OCTINOXATE4Y5P7MUD51ACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTISALATE4X49Y0596WACTIB
ZINC OXIDESOI2LOH54ZACTIM

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
149a6438-3e5c-0d5f-e063-6394a90aae40a893eb63-43ee-4262-9416-f020da3df43c2024-03-26WarningsExact identifier
spl set id: a893eb63-43ee-4262-9416-f020da3df43c

Reported adverse events (FAERS/openFDA)#

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