FDA.reportPublic FDA data

NATURE ORIGIN COLLAGEN BB ORIGINAL

Manufacturer
NATURE REPUBLIC CO., LTD. | Kolmar Korea Co.,LTD. Gwanjeong Factory
Effective date
2021-12-16
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:22:24

Label at a glance#

ProductNATURE ORIGIN COLLAGEN BB ORIGINAL
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: TITANIUM DIOXIDE 6.39%, ETHYLHEXYL METHOXYCINNAMATE 3.00%, ZINC OXIDE 1.92%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: WATER, CYCLOPENTASILOXANE, DIPROPYLENE GLYCOL, GLYCERIN, TALC, PEG-10 DIMETHICONE, DIMETHICONE, ARBUTIN, HEXYLDECYL MYRISTOYL METHYLAMINOPROPIONATE, DISTEARDIMONIUM HECTORITE, ISOEICOSANE, MAGNESIUM SULFATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, C12-14 PARETH-3, SEA WATER, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, PIPER METHYSTICUM LEAF/ROOT/STEM EXTRACT, SILICA, IRON OXIDES(CI 77492), ACRYLATES/DIMETHICONE COPOLYMER, PHENOXYETHANOL, METHICONE, IRON OXIDES(CI 77491), IRON OXIDES(CI 77499), ALUMINUM HYDROXIDE, ALUMINUM STEARATE, BETAINE, ETHYLHEXYLGLYCERIN, FRAGRANCE, SILICA DIMETHYL SILYLATE, TOCOPHERYL ACETATE, ACACIA SENEGAL FLOWER/STEM EXTRACT, ADENOSINE, HYDROGENATED LECITHIN

PURPOSE

OTC - PURPOSE SECTION

Purpose: [UV PROTECTION] This BB Cream with the active ingredient of a plant-based collagen makes the skin firm and supple.

Cautions

WARNINGS SECTION

Cautions: 1. For external use only 2. Avoid contact with eyes and mouth 3. Discontinue use if signs of irritation or rashes appear 4. Keep out of reach of children 5. Replace the cap after use

How to use

DESCRIPTION SECTION

How to use: After completing your basic skincare routine, apply a small amount of the cream to your face using gentle strokes to produce a fresh and natural skin tone.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

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
DIPROPYLENE GLYCOLINACTIVE INGREDIENTE107L85C401
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
51346-36351346-363-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTINOXATE4Y5P7MUD51ACTIB
ZINC OXIDESOI2LOH54ZACTIM
WATER059QF0KO0RIACT
DIPROPYLENE GLYCOLE107L85C40IACT

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 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / TRANSDERMAL296 mgExact identifier — unii candidate
3 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40FILM, EXTENDED RELEASE / BUCCAL30 mgExact identifier — unii candidate
3 equally ranked IID candidates
DIPROPYLENE GLYCOLDIPROPYLENE GLYCOLE107L85C40SYSTEM / TRANSDERMAL6 mgExact identifier — unii candidate
3 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
91718c09-3e1a-42c5-ae1f-f22b9e8eb52a6ab66423-0633-4ff8-a455-2fb1f2f7a5d72023-05-19WarningsExact identifier
spl set id: 6ab66423-0633-4ff8-a455-2fb1f2f7a5d7

Reported adverse events (FAERS/openFDA)#

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