FDA.reportPublic FDA data

CICA FUCOIDAN

Manufacturer
MS Global Bio Co., Ltd.
Effective date
2020-09-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:29:12

Label at a glance#

ProductCICA FUCOIDAN
Active ingredientNIACINAMIDE, WATER
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

niacinamide

OTC - PURPOSE SECTION

anti-wrinkle, whitening

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

WARNINGS SECTION

■ For external use only.Keep out of reach of children. If swallowed, get medical help or contacta Poison Control Center right away. Avoid contact with eyes. Discontinue use if signs of irritation appear

DOSAGE & ADMINISTRATION SECTION

for external use only

INACTIVE INGREDIENT SECTION

Water, Cladosiphon Extract(Fucoidan), Glycerin, Butylene Glycol, Dipropylene Glycol, Niacinamide, Macadamia Ternifolia Seed Oil, Caprylic/Capric Triglyceride, Butylene Glycol, Dicaprylate/Dicaprate, 1,2-Hexanediol, Betaine, Camellia Japonica Seed Oil, Sodium Hyaluronate, Beeswax, Butyrospermum Parkii (Shea) Butter, Cetearyl Alcohol, olysorbate 60, Cetearyl Olivate, Sorbitan Olivate, Cetyl Alcohol, Glyceryl Stearate, PEG-75 Stearate, Ceteth-20, Steareth-20, Hydroxyethylcellulose, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Carbomer, Caprylyl Methicone, Ethylhexylglycerin, Camellia Sinensis Leaf Extract, Aloe Barbadensis Leaf Extract, Centella Asiatica Extract, Lactobacillus/Soybean Ferment Extract, Salix Alba (Willow) Bark Extract, Cinnamomum Cassia Bark Extract, Origanum Vulgare Leaf Extract, Chamaecyparis Obtusa Leaf Extract, Scutellaria Baicalensis Root Extract, Portulaca Oleracea Extract, Adenosine, Flavor, Citronellol, Limonene, Linalool

INDICATIONS & USAGE SECTION

■After water lotion application, dispense an ample amount into your palm. Smooth on the face in gentle rolling motions.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79630-0002-12022-01-28C16284748780-1d6a99b39-7b69-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79630-0002-1CICA FUCOIDAN50 mL in 1 BOTTLECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79630-0002CICA FUCOIDAN (NIACINAMIDE) CREAM [MS GLOBAL BIO CO., LTD.]1Legacy NDC, 1 package rows20200914_af40425a-19ff-5b84-e053-2995a90a03e7.zip

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
79630-000279630-0002-1

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
GLYCERINPDC6A3C0OXIACT
ADENOSINEK72T3FS567IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
NIACINAMIDE25X51I8RD4ACTIB
WATER059QF0KO0RACTIB

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
af403daf-a0a4-7ee5-e053-2a95a90a7342af40425a-19ff-5b84-e053-2995a90a03e72020-09-14WarningsExact identifier
spl id: af403daf-a0a4-7ee5-e053-2a95a90a7342
spl set id: af40425a-19ff-5b84-e053-2995a90a03e7

Reported adverse events (FAERS/openFDA)#

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