FRESH GREEN TEA SEED SERUM

Manufacturer
NATURE REPUBLIC CO., LTD. | Cosmax, Inc
Effective date
2017-02-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:19:31

Label at a glance#

ProductFRESH GREEN TEA SEED SERUM
Active ingredientDIMETHICONE
Label structure8 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: DIMETHICONE (5.00%)

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Camellia Sinensis Leaf Water,Butylene Glycol,Glycerin,Cetyl Ethylhexanoate,Pentylene Glycol,Alcohol Denat.,Water,Ethyl Hexanediol,PEG-32,Diglycerin,Isostearic Acid,PEG-8,PEG-11 Methyl Ether Dimethicone,PEG-60 Hydrogenated Castor Oil,Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Phenoxyethanol,Ammonium Acryloyldimethyltaurate/VP Copolymer,Potassium Hydroxide,Caffeine,Fragrance(Parfum),Xanthan Gum,Camellia Sinensis Seed Oil,Glycine Soja (Soybean) Oil,Benzophenone-9,Disodium EDTA,Sea Water,Yellow 5 (CI 19140),Glycyrrhiza Glabra (Licorice) Root Extract,Centella Asiatica Extract,Chamomilla Recutita (Matricaria) Flower Extract,Yellow 6 (CI 15985),Blue 1 (CI 42090),Portulaca Oleracea Extract,Camellia Sinensis Leaf Extract,Cetearyl Olivate,Sorbitan Olivate

PURPOSE

OTC - PURPOSE SECTION

PURPOSE: [Skin Protectant] Moisture Enriched Cream

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.

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: Gently spread over face.

HOW TO USE

DOSAGE & ADMINISTRATION SECTION

HOW TO USE: Gently spread over face.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51346-342-012021-12-10C16284748780-1ba0f9c33-0d9c-a910-e053-dadaa90a0b85355bf186-d30b-4918-8825-8951c0c6af2f
51346-342-012021-01-29C16284748780-1ba0f9c33-0d9c-a910-e053-dadaa90a0b85355bf186-d30b-4918-8825-8951c0c6af2f

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
DIMETHICONEACTIVE INGREDIENT92RU3N3Y1O1
DIMETHICONEACTIVE MOIETY92RU3N3Y1O1
BUTYLENE GLYCOLINACTIVE INGREDIENT3XUS85K0RA1
CAMELLIA SINENSIS FLOWERINACTIVE INGREDIENT9I2BJY2J171

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51346-34251346-342-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
c0ad3eac-40a7-4108-9316-fb1db1940939355bf186-d30b-4918-8825-8951c0c6af2f2021-12-10WarningsExact identifier
spl set id: 355bf186-d30b-4918-8825-8951c0c6af2f

Reported adverse events (FAERS/openFDA)#

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